Let`s talk about compound :C7H8N2O

About 2-Aminobenzamide, If you have any questions, you can contact Sonawane, AD; Sonawane, RA; Win, KMN; Ninomiya, M; Koketsu, M or concate me.. Name: 2-Aminobenzamide

Name: 2-Aminobenzamide. Recently I am researching about DIORGANYL DISELENIDES SYNTHESIS; C-H ACTIVATION; ELECTROPHILIC CYCLIZATION; IRON(III) CHLORIDE; BETA-PHENYLETHYLAMINES; CATALYZED ANNULATION; TANDEM CYCLIZATION; BOND FORMATION; DERIVATIVES; 2-ALKYNYLBENZALDEHYDES, Saw an article supported by the JSPS KAKENHIMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT)Japan Society for the Promotion of ScienceGrants-in-Aid for Scientific Research (KAKENHI) [17550099]; MEXT: MonbukagakushoMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT). Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Sonawane, AD; Sonawane, RA; Win, KMN; Ninomiya, M; Koketsu, M. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

An efficient, metal free and environment friendly synthesis of isoquinoline-fused benzimidazole has been developed via in situ air oxidation. Also, syntheses of isoquinoline-fused quinazolinone heteroacenes were successfully achieved. The synthesized isoquinoline-fused benzimidazole and isoquinoline-fused quinazolinone derivatives showed lambda(max), F-max and phi(f) values in the ranges 356-394 nm, 403-444 nm and 0.063-0.471, respectively, in CHCl3.

About 2-Aminobenzamide, If you have any questions, you can contact Sonawane, AD; Sonawane, RA; Win, KMN; Ninomiya, M; Koketsu, M or concate me.. Name: 2-Aminobenzamide

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

When did you first realize you had a special interest and talent in2-Aminobenzamide

Application In Synthesis of 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Pismataro, MC; Felicetti, T; Bertagnin, C; Nizi, MG; Bonomini, A; Barreca, ML; Cecchetti, V; Jochmans, D; De Jonghe, S; Neyts, J; Loregian, A; Tabarrini, O; Massari, S or concate me.

An article 1,2,4-Triazolo[1,5-a]pyrimidines: Efficient one-step synthesis and functionalization as influenza polymerase PA-PB1 interaction disruptors WOS:000661282500009 published article about SUBUNIT INTERACTIONS; SMALL-MOLECULE; INHIBITORS; VIRUSES; COMPLEX in [Pismataro, Maria Chiara; Felicetti, Tommaso; Nizi, Maria Giulia; Barreca, Maria Letizia; Cecchetti, Violetta; Tabarrini, Oriana; Massari, Serena] Univ Perugia, Dept Pharmaceut Sci, Via Del Liceo 1, I-06123 Perugia, Italy; [Bertagnin, Chiara; Bonomini, Anna; Loregian, Arianna] Univ Padua, Dept Mol Med, Via Gabelli 63, I-35121 Padua, Italy; [Jochmans, Dirk; De Jonghe, Steven; Neyts, Johan] Katholieke Univ Leuven, Dept Microbiol Immunol & Transplantat, Rega Inst Med Res, Lab Virol & Chemotherapy, Herestr 49,Box 1043, B-3000 Leuven, Belgium in 2021, Cited 46. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Application In Synthesis of 2-Aminobenzamide

In the search for new anti-influenza virus (IV) compounds, we have identified the 1,2,4-triazolo[1,5-a] pyrimidine (TZP) as a very suitable scaffold to obtain compounds able to disrupt IV RNA-dependent RNA polymerase (RdRP) PA-PB1 subunits heterodimerization. In this work, in order to acquire further SAR insights for this class of compounds and identify more potent derivatives, we designed and synthesized additional series of analogues to investigate the role of the substituents around the TZP core. To this aim, we developed four facile and efficient one-step procedures for the synthesis of 5-phenyl-, 6- phenyl- and 7-phenyl-2-amino-[1,2,4]triazolo[1,5-a]pyrimidines, and 2-amino-5-phenyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ol. Two analogues having the ethyl carboxylate moiety at the C-2 position of the TZP were also prepared in good yields. Then, the scaffolds herein synthesized and two previous scaffolds were functionalized and evaluated for their anti-IAV activity, leading to the identification of compound 22 that showed both anti-PA-PB1 (IC50 = 19.5 mM) and anti-IAV activity (EC50 = 16 mM) at non-toxic concentrations, thus resulting among the most active TZP derivatives reported to date by us. A selection of the synthesized compounds, along with a set of in-house available analogues, was also tested against SARS-CoV-2. The most promising compound 49 from this series displayed an EC50 value of 34.47 mM, high-lighting the potential of the TPZ scaffold in the search for anti-CoV agents. (C) 2021 Elsevier Masson SAS. All rights reserved.

Application In Synthesis of 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Pismataro, MC; Felicetti, T; Bertagnin, C; Nizi, MG; Bonomini, A; Barreca, ML; Cecchetti, V; Jochmans, D; De Jonghe, S; Neyts, J; Loregian, A; Tabarrini, O; Massari, S or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

What advice would you give a new faculty member or graduate student interested in a career 88-68-6

Application In Synthesis of 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Dang, MHD; Nguyen, TTM; Nguyen, LHT; Nguyen, TTT; Phan, TB; Tran, PH; Doan, TLH or concate me.

An article Effect of Fe(iii)-based MOFs on the catalytic efficiency of the tandem cyclooxidative reaction between 2-aminobenzamide and alcohols WOS:000564479900023 published article about METAL-ORGANIC FRAMEWORKS; HETEROGENEOUS CATALYST; OXIDATIVE SYNTHESIS; AEROBIC OXIDATION; QUINAZOLINONES; HYDROGENATION; CYTOTOXICITY; SYSTEMS in [Minh-Huy Dinh Dang; Trang Thi Minh Nguyen; Linh Ho Thuy Nguyen; Trang Thi Thu Nguyen; Thang Bach Phan; Tan Le Hoang Doan] Ctr Innovat Mat & Architectures INOMAR, Ho Chi Minh City, Vietnam; [Minh-Huy Dinh Dang; Trang Thi Minh Nguyen; Linh Ho Thuy Nguyen; Trang Thi Thu Nguyen; Thang Bach Phan; Phuong Hoang Tran; Tan Le Hoang Doan] Vietnam Natl Univ Ho Chi Minh City, Ho Chi Minh City, Vietnam; [Phuong Hoang Tran] Univ Sci, Fac Chem, Dept Organ Chem, Ho Chi Minh City, Vietnam in 2020, Cited 63. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Application In Synthesis of 2-Aminobenzamide

The catalytic properties of metal-organic frameworks (MOFs) containing triangular Fe(iii) clusters in the promotion of organic syntheses and photocatalysis applications have been receiving substantial attention for decades. These clusters are appealing due to the strong Lewis acidity afforded by coordinatively unsaturated sites upon the removal of solvent from the framework. In this paper, triangular Fe(iii) cluster-based MOFs were shown to be highly efficient heterogeneous catalysts for the solvent-free one-pot condensation of 2-aminobenzamide and alcohols to form quinazolin-4-ones under microwave irradiation. The Fe-MOF catalysts ranging from microporous to mesoporous structures with a variety of geometrical pore structures were investigated. Because of the open accessible spaces for reactants and high density of active sites, MOF-907, built from trimer Fe clusters and a mixture of two linkers, was more effective than other Fe(iii)-MOFs. The catalyst can be used for a broad substrate scope and recycled several times without a significant drop-off in its activity.

Application In Synthesis of 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Dang, MHD; Nguyen, TTM; Nguyen, LHT; Nguyen, TTT; Phan, TB; Tran, PH; Doan, TLH or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

Top Picks: new discover of 88-68-6

About 2-Aminobenzamide, If you have any questions, you can contact Zima, V; Albinana, CB; Rojikova, K; Pokorna, J; Pachl, P; Rezacova, P; Hudlicky, J; Navratil, V; Majer, P; Konvalinka, J; Kozisek, M; Machara, A or concate me.. Safety of 2-Aminobenzamide

Zima, V; Albinana, CB; Rojikova, K; Pokorna, J; Pachl, P; Rezacova, P; Hudlicky, J; Navratil, V; Majer, P; Konvalinka, J; Kozisek, M; Machara, A in [Zima, Vaclav; Albinana, Carlos Berenguer; Hudlicky, Jason; Machara, Ales] Charles Univ Prague, Fac Sci, Dept Organ Chem, Hlavova 8, Prague 12800 2, Czech Republic; [Zima, Vaclav; Albinana, Carlos Berenguer; Rojikova, Katerina; Pokorna, Jana; Pachl, Petr; Rezacova, Pavlina; Hudlicky, Jason; Navratil, Vaclav; Majer, Pavel; Konvalinka, Jan; Kozisek, Milan; Machara, Ales] Gilead Sci, Czech Acad Sci, Inst Organ Chem & Biochem, Flemingovo 2, Prague 16610 6, Czech Republic; [Zima, Vaclav; Albinana, Carlos Berenguer; Rojikova, Katerina; Pokorna, Jana; Pachl, Petr; Rezacova, Pavlina; Hudlicky, Jason; Navratil, Vaclav; Majer, Pavel; Konvalinka, Jan; Kozisek, Milan; Machara, Ales] IOCB Res Ctr, Flemingovo 2, Prague 16610 6, Czech Republic; [Rojikova, Katerina] Charles Univ Prague, Fac Med 1, Katerinska 1660-32, Prague 12108, Czech Republic; [Rezacova, Pavlina] Acad Sci Czech Republ, Inst Mol Genet, Videnska 1083, Prague 14000 4, Czech Republic; [Konvalinka, Jan] Charles Univ Prague, Fac Sci, Dept Biochem, Hlavova 8, Prague 12800 2, Czech Republic published Investigation of flexibility of neuraminidase 150-loop using tamiflu derivatives in influenza A viruses H1N1 and H5N1 in 2019, Cited 62. Safety of 2-Aminobenzamide. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

This study focuses on design, synthesis and in vitro evaluation of inhibitory potency of two series of sialylmimetic that target an exosite (150-cavity) adjacent to the active site of influenza neuraminidases from A/California/07/2009 (H1N1) pandemic strain and A/chicken/Nakorn-Patom/Thailand/CU-K2-2004 (H5N1). The structure-activity analysis as well as 3-D structure of the complex of parental compound with the pandemic neuraminidase p09N1 revealed high flexibility of the 150-cavity towards various modification of the neuraminidase inhibitors. Furthermore, our comparison of two methods for inhibition constant determination performed at slightly different pH values suggest that the experimental conditions of the measurement could dramatically influence the outcome of the analysis in the compound-dependent manner. Therefore, previously reported Ki values determined at non-physiological pH should be carefully scrutinized.

About 2-Aminobenzamide, If you have any questions, you can contact Zima, V; Albinana, CB; Rojikova, K; Pokorna, J; Pachl, P; Rezacova, P; Hudlicky, J; Navratil, V; Majer, P; Konvalinka, J; Kozisek, M; Machara, A or concate me.. Safety of 2-Aminobenzamide

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

Our Top Choice Compound:88-68-6

Quality Control of 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Machushynets, NV; Wu, CS; Elsayed, SS; Hankemeier, T; van Wezel, GP or concate me.

An article Discovery of novel glycerolated quinazolinones from Streptomyces sp. MBT27 WOS:000460642800021 published article about COMPLETE GENOME SEQUENCE; NATURAL-PRODUCTS; ANTIBIOTIC PRODUCTION; SECONDARY METABOLISM; MASS-SPECTROMETRY; MOLECULAR NETWORKING; PATHOGENS; PLATFORM; STRESS; LINKS in [Machushynets, Nataliia V.; Wu, Changsheng; Elsayed, Somayah S.; van Wezel, Gilles P.] Leiden Univ, Inst Biol, Mol Biotechnol, Sylviusweg 72, NL-2333 BE Leiden, Netherlands; [Wu, Changsheng] Shandong Univ, Inst Microbial Technol, State Key Lab Microbial Technol, Qingdao 266237, Peoples R China; [Hankemeier, Thomas] Leiden Univ, LACDR, Einsteinweg 55, NL-2333 CC Leiden, Netherlands in 2019, Cited 57. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Quality Control of 2-Aminobenzamide

Actinobacteria are a major source of novel bioactive natural products. A challenge in the screening of these microorganisms lies in finding the favorable growth conditions for secondary metabolite production and dereplication of known molecules. Here, we report that Streptomyces sp. MBT27 produces 4-quinazolinone alkaloids in response to elevated levels of glycerol, whereby quinazolinones A (1) and B (2) form a new sub-class of this interesting family of natural products. Global Natural Product Social molecular networking (GNPS) resulted in a quinazolinone-related network that included anthranilic acid (3), anthranilamide (4), 4(3H)-quinazolinone (5), and 2,2-dimethyl-1,2-dihydroquinazolin-4(3H)-one (6). Actinomycins D (7) and X2 (8) were also identified in the extracts of Streptomyces sp. MBT27. The induction of quinazolinone production by glycerol combined with biosynthetic insights provide evidence that glycerol is integrated into the chemical scaffold. The unprecedented 1,4-dioxepane ring, that is spiro-fused into the quinazolinone backbone, is most likely formed by intermolecular etherification of two units of glycerol. Our work underlines the importance of varying the growth conditions for the discovery of novel natural products and for understanding their biosynthesis.

Quality Control of 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Machushynets, NV; Wu, CS; Elsayed, SS; Hankemeier, T; van Wezel, GP or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

New explortion of 64-10-8

About 1-Phenylurea, If you have any questions, you can contact Dan, YT; Ji, MY; Tao, SP; Luo, G; Shen, Z; Zhang, YL; Sang, WJ or concate me.. COA of Formula: C7H8N2O

Authors Dan, YT; Ji, MY; Tao, SP; Luo, G; Shen, Z; Zhang, YL; Sang, WJ in ELSEVIER published article about in [Dan, Yitong; Ji, Mengyuan; Sang, Wenjing] Donghua Univ, Coll Environm Sci & Engn, Text Pollut Controlling Engn Ctr, Minist Environm Protect, Shanghai 201620, Peoples R China; [Tao, Shuping; Shen, Zheng; Zhang, Yalei] Tongji Univ, Natl Engn Res Ctr Protected Agr, Inst New Rural Dev, Shanghai 200092, Peoples R China; [Luo, Gang] Fudan Univ, Dept Environm Sci & Engn, Shanghai Key Lab Atmospher Particle Pollut & Prev, Shanghai 200433, Peoples R China in 2021.0, Cited 76.0. COA of Formula: C7H8N2O. The Name is 1-Phenylurea. Through research, I have a further understanding and discovery of 64-10-8

The application of phenylurea herbicides (PUHs) may lead to the extensive distribution in soils, while the role of straw biochar as a soil amendment on the transport and sorption of PUHs are still unclear. Thus, the transport and sorption behavior of three typical PUHs with rice straw biochar (RSB) was studied in both adsorption simulation experiments of aqueous solution and packed column experiments:the sorption mechanism of RSB to herbicides was investigated through batch sorption studies with three influencing factors including dosage of RSB, pH, and ionic strength (IS) with orthogonal test. The sorption coeff icients were improved significantly by increasing the dosage of RSB, while there was no obvious influence by enhancing the pH and IS value. The optimal sorption conditions (pH value at 3, IS at 0.1 M, and RSB dosage at 60 mg) of three herbicides were set and the maximum removal rates of Monuron, Diuron, and Linuron were 41.9%, 25%, and 56.8%, respectively. The co-transport process of RSB and PUHs were investigated under different RSB dosage, pH value, and IS value. The retention effect increased greatly with enhancing the RSB dosage and pH value. However, IS did not have a significant influence on the retention of RSB, and therefore it had little effect on the adsorption capacity, which was consistent with the results of sorption experiments. The breakthrough curves (BTCs) for co-transport were well simulated by the two-site non-equilibrium convection-dispersion equation (CDE). Most of the regression coefficients (R-2) were above 0.99, which uncovered the co-transport in packed column were affected by physical absorption and chemical forces. According to the fitting parameters analysis, the RSB particles and PUHs were subjected to a greater resistance and a stronger stability by reducing pH value in porous media. The presence of RSB increased the amount of dynamic sorption sites in the entire co-transport system, which led to a significant promotion of the PUHs’ sorption and interception. (C) 2021 Elsevier B.V. All rights reserved.

About 1-Phenylurea, If you have any questions, you can contact Dan, YT; Ji, MY; Tao, SP; Luo, G; Shen, Z; Zhang, YL; Sang, WJ or concate me.. COA of Formula: C7H8N2O

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

Chemical Research in 2-Aminobenzamide

Computed Properties of C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Huang, HY; Lin, XY; Yen, SY; Liang, CF or concate me.

An article Facile access toN-formyl imide as anN-formylating agent for the direct synthesis ofN-formamides, benzimidazoles and quinazolinones WOS:000553219600023 published article about ACID-CATALYZED TRANSAMIDATION; N-SUBSTITUTED FORMAMIDES; CARBON-DIOXIDE; EFFICIENT SYNTHESIS; AMINES; DERIVATIVES; CARBOXAMIDES; METHANOL; OXIDATION; CO2 in [Huang, Hsin-Yi; Lin, Xiu-Yi; Yen, Shih-Yao; Liang, Chien-Fu] Natl Chung Hsing Univ, Dept Chem, Taichung 402, Taiwan in 2020, Cited 91. Computed Properties of C7H8N2O. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

N-Formamide synthesis usingN-formyl imide with primary and secondary amines with catalytic amounts ofp-toluenesulfonic acid monohydrate (TsOH center dot H2O) is described. This reaction is performed in water without the use of surfactants. Moreover,N-formyl imide is efficiently synthesized using acylamidines with TsOH center dot H2O in water. In addition,N-formyl imide was successfully used as a carbonyl source in the synthesis of benzimidazole and quinazolinone derivatives. Notable features ofN-formylation of amines by usingN-formyl imide include operational simplicity, oxidant- and metal-free conditions, structurally diverse products, and easy applicability to gram-scale operation.

Computed Properties of C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Huang, HY; Lin, XY; Yen, SY; Liang, CF or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

What I Wish Everyone Knew About 88-68-6

SDS of cas: 88-68-6. About 2-Aminobenzamide, If you have any questions, you can contact Guo, YB; Gao, ZH; Li, JC; Bi, XJ; Shi, EX; Xiao, JH or concate me.

Authors Guo, YB; Gao, ZH; Li, JC; Bi, XJ; Shi, EX; Xiao, JH in ROYAL SOC CHEMISTRY published article about in [Guo, Yongbiao; Gao, Zhenhua; Li, Junchen; Bi, Xiaojing; Shi, Enxue; Xiao, Junhua] State Key Lab NBC Protect Civilian, Beijing, Peoples R China in 2021, Cited 30. SDS of cas: 88-68-6. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

Herein, we report on the highly efficient and practical synthesis of 2,3-dihydroquinazolinones directly from diverse aldehydes with excellent yields and enantioselectivity. Particularly, this protocol affords better enantiocontrol for aliphatic aldehydes (up to 99% yield, 97% ee), which always gave unsatisfactory results in the previous studies. Moreover, this catalytic system shows wide tolerance to different functional groups such as alkenyl, nitro and halogens. Most importantly, its practicability is well elucidated via the gram-scale synthesis of different types of products at 0.1 mol% catalyst loading and the simplified work-up procedure. To better understand the reaction pathway and origin of the enantioselectivity, DFT calculations were also performed.

SDS of cas: 88-68-6. About 2-Aminobenzamide, If you have any questions, you can contact Guo, YB; Gao, ZH; Li, JC; Bi, XJ; Shi, EX; Xiao, JH or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

What Kind of Chemistry Facts Are We Going to Learn About C7H8N2O

Safety of 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Lehmann, DM; Camp, AA or concate me.

Lehmann, DM; Camp, AA in [Lehmann, David M.] US EPA, Ctr Publ Hlth & Environm Assessment CPHEA, Hlth & Environm Effects Assessment Div, Integrated Hlth Assessment Branch, Durham, NC 27709 USA; [Camp, Allison A.] Oak Ridge Associated Univ, Oak Ridge, TN USA published A systematic scoping review of the methodological approaches and effects of pesticide exposure on solitary bees in 2021, Cited 108. Safety of 2-Aminobenzamide. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

Background Pollination services provided by solitary bees, the largest group of bees worldwide, are critical to the vitality of ecosystems and agricultural systems alike. Disconcertingly, bee populations are in decline, and while no single causative factor has been identified, pesticides are believed to play a role in downward population trends. The effects of pesticides on solitary bee species have not been previously systematically cataloged and reviewed. Objectives This systematic scoping review examines available evidence for effects of pesticide exposure on solitary bees to identify data gaps and priority research needs. Methods A systematic literature search strategy was developed to identify and document reports on solitary bee pesticide exposure-effects investigations. Literature was subsequently screened for relevance using a Population, Exposures, Comparators, and Outcomes (PECO) statement and organized into a systematic evidence map. Investigations were organized by effect category (lethal effects on immatures, lethal effects on adults, sublethal effects on immatures, and sublethal effects on adults), species, pesticide class, and publication year. Results A comprehensive literature search of Web of Science and ProQuest Agricultural & Environmental Science supplemented by targeted internet searching and reference mining yielded 176 reports and publications for title and abstract screening and 65 that met PECO criteria (22 included lethal and 43 included sublethal effects endpoints). Relevant design details (pesticide, test compound configuration, study type, species, sex, exposure duration) were extracted into literature inventory tables to reveal the extent endpoints have been investigated and areas in need of additional research. Conclusions Evidence mapping revealed diversity in the pesticides and endpoints studied across the database. However, dilution across bee species, lack of complementary laboratory work and paucity of replicated investigations complicate efforts to interpret and apply available data to support pesticide risk assessment.

Safety of 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Lehmann, DM; Camp, AA or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

Let`s talk about compound :2-Aminobenzamide

About 2-Aminobenzamide, If you have any questions, you can contact Brenz, F; Linke, S; Simat, TJ or concate me.. Formula: C7H8N2O

An article Linear and cyclic oligomers in PET, glycol-modified PET and Tritan (TM) used for food contact materials WOS:000590108700001 published article about POLYETHYLENE TEREPHTHALATE PET; IDENTIFICATION; MIGRATION; POLY(ETHYLENE-TEREPHTHALATE); QUANTIFICATION; POLYMERIZATION; POLYESTERS; MONOMERS in [Brenz, Fabrian; Linke, Susanne; Simat, Thomas J.] Tech Univ Dresden, Dept Chem & Food Chem, Chair Food Sci & Food Contact Mat, Dresden, Germany in 2021, Cited 39. Formula: C7H8N2O. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

Polyesters are commonly used as food contact materials. During manufacture of polyesters different low molecular mass oligomers (<1000 Da) are formed in the polymer melt. These so-called non-intentionally added substances (NIAS) are potential migrants into foods. In this work, different polyester samples made of polyethylene terephthalate (PET), glycol-modified PET (PETG) and Tritan (TM) were investigated on their qualitative and quantitative oligomer composition. The analysis of acetonitrile extracts by HPLC-DAD/ESI-MS revealed the presence of about 100 linear (different combinations of hydroxyl-, carboxyl-, methyl ester end groups) and cyclic oligomers depending on the main and co-monomers. The identified oligomers were quantified in different extracts and after reprecipitation by HPLC-DAD using bis-hydroxyethylene terephthalate (BHET) as external standard. The amount of oligomers isolated by reprecipitation ranged between 0.80 and 3.4% in the respective polyester. Cyclic oligomers generally made up 90% or more of the isolated oligomers. Compared to the exhaustive extracts the leaching of oligomers into 20% ethanol (1 h, 60 degrees C) resulted in a considerable change of the oligomer distribution with a predominant detection of linear oligomers. This suggests linear oligomers to be relevant for migration into aqueous foods despite the dominant amount of extractable cyclic oligomers in polyesters. Analysis of the extractable oligomers of a PET preform and a PETG container and their corresponding raw material pellets revealed that the injection moulding process did not significantly change the amount of cyclic oligomers but did increase the amount of low molecular mass linear oligomers about twofold. About 2-Aminobenzamide, If you have any questions, you can contact Brenz, F; Linke, S; Simat, TJ or concate me.. Formula: C7H8N2O

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem