Tag: M.W=100-150

Recommanded Product: 1-Phenylurea. In 2020.0 J CHROMATOGR A published article about LIQUID-CHROMATOGRAPHY; CLASSIFICATION; PURIFICATION; SELECTIVITY; RETENTION; SYSTEM; SFC in [Jiang, Dasen; Ke, Yanxiong; Cai, Jianfeng; Zhang, Huanhuan; Fu, Qing; Jin, Yu; Liang, Xinmiao] East China Univ Sci & Technol, Engn Res Ctr Pharmaceut Proc Chem, Sch Pharm, Minist Educ, Shanghai 200237, Peoples R China; [Liang, Xinmiao] Chinese Acad Sci, Dalian Inst Chem Phys, Key Lab Separat Sci Analyt Chem, Key Lab Nat Med, Dalian 116023, Liaoning, Peoples R China in 2020.0, Cited 29.0. The Name is 1-Phenylurea. Through research, I have a further understanding and discovery of 64-10-8.

In recent years, supercritical fluid chromatography (SFC) has become a powerful tool in modern analytical chemistry, and the diversity of stationary phases in SFC promotes phenyl-type phases to confront with a significant resurgence of interest. In this paper, a series of phenyl-type stationary phases with different substituted benzenes involving N-propylbenzamide (PB), 4-fluoro-N-propylbenzamide (PB-F), and 4-ethyl-N-propylbenzamide (PB-ET) were synthesized. Retention mechanism of these phases in SFC was investigated using a linear solvation energy relationship (LSER) model. The phenyl-type stationary phases with all positive parameters can provide all types of interaction, typically involving hydrogen bonding, dipole-dipole and dispersive interactions. The different benzene’s substituents of the stationary phases mainly affected their hydrogen bonding and dipole-dipole interactions, which could be reflected by the angle between the solvation vectors to some extent. The k-k plot showed that the selectivity difference of phenyl-type stationary phases was closely related to the type of solute. Thus, based on twenty-five natural phenolic compounds, two systems with high orthogonality (63.49%) were constructed using three columns, namely phenyl column (PHE) x PB-F and PB x PB-F. Finally, after investigating the influence of chromatographic conditions, ten flavonoids could be separated by using PB, PB-F and PHE columns in SFC. (C) 2019 Published by Elsevier B.V.

Recommanded Product: 1-Phenylurea. About 1-Phenylurea, If you have any questions, you can contact Jiang, DS; Ke, YX; Cai, JF; Zhang, HH; Fu, Q; Jin, Y; Liang, XM or concate me.

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

In 2020 ORG BIOMOL CHEM 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. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Name: 2-Aminobenzamide

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.

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Reference:
Thiomorpholine – Wikipedia,
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Dai, ZS; Tian, QQ; Li, YW; Shang, SQ; Luo, W; Wang, XT; Li, D; Zhang, Y; Li, ZY; Yuan, JY in [Dai, Zeshu; Tian, Qingqiang; Li, Yanwu; Shang, Suqin; Luo, Wen; Wang, Xuetong; Li, Dan; Zhang, Ying; Li, Zhiyao; Yuan, Jianyong] Chongqing Med Univ, Coll Pharm, Dept Med Chem, Chongqing 400016, Peoples R China published Michael Addition Reaction Catalyzed by Imidazolium Chloride to Protect Amino Groups and Construct Medium Ring Heterocycles in 2019, Cited 53. HPLC of Formula: C7H8N2O. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

An effective approach for amino protection and construction of a seven-membered ring has been developed. The method uses imidazolium chloride to carry out the Michael addition reaction at low temperatures and perform amino deprotection or construction of a seven-membered ring at high temperatures.

HPLC of Formula: C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Dai, ZS; Tian, QQ; Li, YW; Shang, SQ; Luo, W; Wang, XT; Li, D; Zhang, Y; Li, ZY; Yuan, JY or concate me.

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

Category: thiomorpholine. In 2019 GREEN CHEM published article about C-H BOND; CARBON-MONOXIDE SOURCE; CATALYZED SYNTHESIS; DIMETHYL-SULFOXIDE; ALPHA-METHYLATION; FACILE SYNTHESIS; GREEN CHEMISTRY; TERTIARY-AMINES; SITU GENERATION; BUILDING-BLOCK in [Senadi, Gopal Chandru; Kudale, Vishal Suresh; Wang, Jeh-Jeng] Kaohsiung Med Univ, Dept Med & Appl Chem, 100,Shiquan 1st Rd, Kaohsiung 807, Taiwan; [Wang, Jeh-Jeng] Kaohsiung Med Univ Hosp, Dept Med Res, 100,Tzyou 1st Rd, Kaohsiung 807, Taiwan; [Senadi, Gopal Chandru] SRM Inst Sci & Technol, Dept Chem, Chennai 603203, Tamil Nadu, India in 2019, Cited 132. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

Alcohols and ethers were identified as sustainable methine sources for synthesizing quinazolinone and benzimidazole derivatives using a combination of TsOHH2O/O-2 and appropriate bis-nucleophiles for the first time. Deuterium labeling studies clearly proved that the C-2 hydrogen of the synthesized heterocycles came from the methine source. These unique reaction conditions were successfully applied to the synthesis of echinozolinone (2e), 2f (a common precursor of rutaecarpine and (+/-) evodiamine), and dimedazole (6d). Notable features of this method include its low toxicity, use of commercial feedstocks as substrates, low cost, broad functional group tolerance and suitability for a wide range of bis-nucleophilic starting materials.

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

COA of Formula: C7H8N2O. Authors Yang, L; Hou, HQ; Li, L; Wang, J; Zhou, SY; Wu, M; Ke, F in ROYAL SOC CHEMISTRY published article about in [Yang, Li; Li, Lan; Ke, Fang] Yibin Univ, Coll Chem & Chem Engn, Yibin, Sichuan, Peoples R China; [Hou, Huiqing; Wang, Jin; Zhou, Sunying; Wu, Mei; Ke, Fang] Fujian Med Univ, Fuzhou, Fujian, Peoples R China in 2021, Cited 64. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

An efficient and practical electrochemically catalyzed transition metal-free process for the synthesis of substituted quinazolinones from simple and readily available o-aminobenzonitriles and aldehydes in water has been accomplished. I-2/base and water play an unprecedented and vital role in the reaction. By electrochemically catalysed hydrolysis of o-aminobenzonitriles, the synthesis of quinazolinones with benzaldehyde was first proposed. The synthetic utility of this method was demonstrated by gram-scale operation, as well as the preparation of bioactive N-(2,5-dichlorophenyl)-6-(2,2,2-trifluoroethoxy) pteridin-4-amine, which enables straightforward, practical and environmentally benign quinazolinone formation.

COA of Formula: C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Yang, L; Hou, HQ; Li, L; Wang, J; Zhou, SY; Wu, M; Ke, F or concate me.

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Thiomorpholine – Wikipedia,
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Name: 1-Phenylurea. In 2020.0 MOLECULES published article about GAS-CHROMATOGRAPHY; FRUITS; PROCYMIDONE; CUCUMBERS; PROVINCE; CARBARYL; STORAGE; FOODS; CHINA in [Ramadan, Mohamed F. A.] Agr Res Ctr, Pesticide Anal Res Dept, Cent Agr Pesticide Lab, Dokki 12618, Egypt; [Ramadan, Mohamed F. A.; Abdel-Hamid, Mohamed M. A.; Altorgoman, Montasser M. F.] Abha Food Safety Lab, Abha 61421, Saudi Arabia; [Abdel-Hamid, Mohamed M. A.] Alexandria Univ, Fac Sci, Dept Chem, Alexandria 21524, Egypt; [Altorgoman, Montasser M. F.] Alexandria Univ, Fac Sci, Dept Biochem, Alexandria 51521, Egypt; [AlGaramah, Hamed A.; Awwad, Nasser S.] King Khalid Univ, RCAMS, POB 9004, Abha 61413, Saudi Arabia; [Alawi, Mohammed A.] Inspect & License Dept Asir Municipal, Abha 61421, Saudi Arabia; [Shati, Ali A.] King Khalid Univ, Fac Sci, Biol Dept, Abha 9004, Saudi Arabia; [Shweeta, Hoda A.] Umm Al Qura Univ, Coll Pharm, POB 715, Mecca 21955, Saudi Arabia in 2020.0, Cited 46.0. The Name is 1-Phenylurea. Through research, I have a further understanding and discovery of 64-10-8.

This study’s aim was to determine the pesticide residues in 10 different vegetable commodities from the Asir region, Saudi Arabia. We evaluated 211 vegetable samples, collected from supermarkets between March 2018 and September 2018, for a total of 80 different pesticides using ultrahigh-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) and gas chromatography-tandem mass spectrometry (GC-MS/MS) after extraction with a multi-residue method (the QuEChERS method). The results were assessed according to the maximum residue limit (MRL) provided by European regulations for each pesticide in each commodity. All lettuce, cauliflower, and carrot samples were found to be free from pesticide residues. A total of 145 samples (68.7%) contained detectable pesticide residues at or lower than MRLs, and 44 samples (20.9%) contained detectable pesticide residues above MRLs. MRL values were exceeded most often in chili pepper (14 samples) and cucumber (10 samples). Methomyl, imidacloprid, metalaxyl, and cyproconazole were the most frequently detected pesticides. Based on the results of this study, we recommend that a government-supported program for the monitoring of pesticide residues in vegetables be established to promote consumers’ health and achieve sustainable farming systems.

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Reference:
Thiomorpholine – Wikipedia,
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I found the field of Environmental Sciences & Ecology very interesting. Saw the article Improvement of pesticide removal in contaminated media using aqueous extracts from contaminated biopurification systems published in 2019.0. COA of Formula: C7H8N2O, Reprint Addresses Romero, E (corresponding author), CSIC, EEZ, Dept Environm Protect, C Prof Albareda 1, E-18008 Granada, Spain.. The CAS is 64-10-8. Through research, I have a further understanding and discovery of 1-Phenylurea

Despite certain limitations, bioaugmentation enhances the efficiency of bioremediation systems. In this study, three aqueous extracts (APE, ACE and APE) from aged residual biomixtures in three biopurification systems (BPSs) exposed to pesticides at a pilot scale were found to improve pesticide removal. The addition of ACEs and AVEs to solutions containing the model compound diuron increased removal rates 6- and 17-fold, respectively, as compared to APEs. These extracts also increased the removal of the metabolite 3,4-dichloroaniline, while AVEs, in particular, were found to remove all pesticides within 9 days. Three metabolites less hazardous than 3,4-dichloroaniline were identified by SPME/GC/MS. AVEs, which also enhance linuron removal in liquid media, were found to increase diuron removal 6-fold in BPSs. We observed an increase in the relative abundance of taxa, such as Chloroflexi, Acidobacteria, Gemmatimonadetes, Firmicutes, Deinococcus-Thermus and especially Proteobacteria (10%), in AV biomixtures, as well as an enrichment of gamma-proteobacteria and the actinobacterial genus Dokdonella in AVEs with respect to initial noncontaminated IV biomixture. We demonstrate that extracts containing a pollutant-acclimatized microbiome could be used as part of a bioaugmentation strategy to improve the functioning of on-farm BPSs and contaminated systems. (c) 2019 Elsevier B.V. All rights reserved.

COA of Formula: C7H8N2O. About 1-Phenylurea, If you have any questions, you can contact Romero, IA; van Dillewijn, P; Nesme, J; Sorensen, SJ; Romero, E or concate me.

Reference:
Thiomorpholine – Wikipedia,
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An article Iridium(III)-Catalyzed Alkynylation of 2-(Hetero)arylquinazolin-4-one Scaffolds via C-H Bond Activation WOS:000460491600052 published article about CROSS-COUPLING REACTION; TERMINAL ALKYNES; ETHYNYL BENZIODOXOLONES; CATALYZED ALKYNYLATION; SONOGASHIRA REACTIONS; ARENES; QUINAZOLINONE; AMIDATION; ACETYLENE; AMINATION in [Rohokale, Rajendra S.; Kalshetti, Rupali G.; Ramana, Chepuri V.] CSIR Natl Chem Lab, Div Organ Chem, Dr Homi Bhabha Rd, Pune 411008, Maharashtra, India; [Kalshetti, Rupali G.; Ramana, Chepuri V.] Acad Sci & Innovat Res, New Delhi 110025, India in 2019, Cited 80. Application In Synthesis of 2-Aminobenzamide. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

The directed C-H alkynylation of 2-(hetero)arylquinazolin-4-ones has been explored with the ethynylbenziodoxolone reagent TIPS-EBX employing an Ir(III) catalyst. Complementary conditions for either monoalkynylation or dialkynylation have been developed. Also demonstrated is the broad scope of this reaction and the compatibility of various functional groups such as -F, -Cl, -Br, -CF3, -OMe, -NO2, and alkyl, etc.

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

Product Details of 64-10-8. Authors Abdourahime, H; Anastassiadou, M; Brancato, A; Brocca, D; Cabrera, LC; De Lentdecker, C; Ferreira, L; Greco, L; Jarrah, S; Kardassi, D; Leuschner, R; Lostia, A; Lythgo, C; Medina, P; Miron, I; Molnar, T; Nave, S; Pedersen, R; Raczyk, M; Reich, H; Ruocco, S; Sacchi, A; Santos, M; Stanek, A; Sturma, J; Tarazona, J; Theobald, A; Vagenende, B; Verani, A; Villamar-Bouza, L in EUROPEAN FOOD SAFETY AUTHORITY-EFSA published article about in in 2019.0, Cited 16.0. The Name is 1-Phenylurea. Through research, I have a further understanding and discovery of 64-10-8

According to Article 12 of Regulation (EC) No396/2005, EFSA has reviewed the maximum residue levels (MRLs) currently established at European level for the pesticide active substance fluometuron. To assess the occurrence of fluometuron residues in plants, processed commodities, rotational crops and livestock, EFSA considered the conclusions derived in the framework of Commission Regulation (EC) No33/2008 as well as the European authorisations reported by Member States (including the supporting residues data). Based on the assessment of the available data, an MRL proposal was derived and a consumer risk assessment was carried out. All information required by the regulatory framework was present and a risk to consumers was not identified. In addition, EFSA identified some data gaps which are not expected to impact on the validity of the MRL derived but which might have an impact on national authorisations.

Product Details of 64-10-8. About 1-Phenylurea, If you have any questions, you can contact Abdourahime, H; Anastassiadou, M; Brancato, A; Brocca, D; Cabrera, LC; De Lentdecker, C; Ferreira, L; Greco, L; Jarrah, S; Kardassi, D; Leuschner, R; Lostia, A; Lythgo, C; Medina, P; Miron, I; Molnar, T; Nave, S; Pedersen, R; Raczyk, M; Reich, H; Ruocco, S; Sacchi, A; Santos, M; Stanek, A; Sturma, J; Tarazona, J; Theobald, A; Vagenende, B; Verani, A; Villamar-Bouza, L or concate me.

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

Recently I am researching about MONOCLONAL-ANTIBODY; POTENT; ACTIVATION; MODERATE; SIGNAL; ROLES; OPTIMIZATION; USTEKINUMAB; MOLECULES; DISCOVERY, Saw an article supported by the Bristol-Myers Squibb CompanyBristol-Myers Squibb. COA of Formula: C7H8N2O. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Moslin, R; Zhang, YL; Wrobleski, ST; Lin, SQ; Mertzman, M; Spergel, S; Tokarski, JS; Strnad, J; Gillooly, K; McIntyre, KW; Zupa-Fernandez, A; Cheng, LH; Sun, HD; Chaudhry, C; Huang, C; D’Arienzo, C; Heimrich, E; Yang, XX; Muckelbauer, JK; Chang, C; Tredup, J; Mulligan, D; Xie, DL; Aranibar, N; Chiney, M; Burke, JR; Lombardo, L; Carter, PH; Weinstein, DS. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

As a member of the Janus OAK) family of nonreceptor tyrosine kinases, TYK2 plays an important role in mediating the signaling of pro-inflammatory cytokines including IL-12, IL-23, and type 1 interferons. The nicotinamide 4, identified by a SPA-based high-throughput screen targeting the TYK2 pseudokinase domain, potently inhibits IL-23 and IFN alpha signaling in cellular assays. The described work details the optimization of this poorly selective hit (4) to potent and selective molecules such as 47 and 48. The discoveries described herein were critical to the eventual identification of the clinical TYK2 JH2 inhibitor (see following report in this issue). Compound 48 provided robust inhibition in a mouse IL-12-induced IFN gamma pharmacodynamic model as well as efficacy in an IL-23 and IL-12-dependent mouse colitis model. These results demonstrate the ability of TYK2 JH2 domain binders to provide a highly selective alternative to conventional TYK2 orthosteric inhibitors.

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