Heterocyclic Building Blocks-Thiomorpholine

Authors Ghosh, T; Mohammad, A; Mobin, SM in AMER CHEMICAL SOC published article about PALLADIUM-CATALYZED CYANATION; AEROBIC OXIDATIVE CONVERSION; REDUCTIVE AMINATION; HIGHLY EFFICIENT; ARYL BROMIDES; NITRILES; ALDEHYDES; ACID; NANOPARTICLES; ALCOHOLS in [Ghosh, Topi; Mohammad, Akbar; Mobin, Shaikh M.] Indian Inst Technol Indore, Discipline Chem, Khandwa Rd, Indore 453552, Madhya Pradesh, India; [Mobin, Shaikh M.] Indian Inst Technol Indore, Discipline Met Engn & Mat Sci, Khandwa Rd, Indore 453552, Madhya Pradesh, India; [Mobin, Shaikh M.] Indian Inst Technol Indore, Discipline Biosci & Biomed Engn, Khandwa Rd, Indore 453552, Madhya Pradesh, India in 2019, Cited 91. Recommanded Product: 104-21-2. The Name is 4-Methoxybenzyl acetate. Through research, I have a further understanding and discovery of 104-21-2

Development of a low-cost, environmentally benign and robust catalyst for multipurpose industrially relevant organic transformations is highly desirable for the sustainable future of chemical industries. A hybrid cobalt doped-cerium oxide nanocatalyst (Co@CeO2NC) was prepared via simple coprecipitation method using water as the solvent. The characterization of Co@CeO2NC was performed using different techniques such as XRD, TGA, FE-SEM, HR-TEM, EDAX-mapping, BET, and XPS analysis. The structural characterization of the prepared sample by XRD and XPS analysis revealed the presence of the mixed phase of cobalt oxide and cobalt doped-cerium oxide as a hybrid (Co@CeO2NC). Industrially relevant organic transformations such as (i) nitrile formation using aldehyde with hydroxyl amine hydrochloride, (ii) reductive amination of aldehydes to form tertiary N,N-dimethyl amines, and (iii) direct acetylation of alcohols/amines with acetic acid were achieved in an excellent manner using Co@CeO2NC hybrid as the multifunctional catalyst. Excellent catalytic activity of Co@CeO2NC was noticed for the conversion of 4-chlorobenzaldehyde to 4-chlorobenzonitrile with 99% conversion and 99% selectivity and 100% conversion of benzaldehyde to N,N-dimethylbenzylamine using DMF as NMe2 source, reductant, and solvent. Moreover, acetylation of 4-methoxybenzyl alcohol and 2-methyl aniline gave excellent conversion and selectivity toward the formation of -O and -N acetyl. The scope of the Co@CeO2NC was further evaluated for other aldehydes, alcohols, and amines with an excellent conversion and high selectivity.

About 4-Methoxybenzyl acetate, If you have any questions, you can contact Ghosh, T; Mohammad, A; Mobin, SM or concate me.. Recommanded Product: 104-21-2

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

Recommanded Product: 99-61-6. Recently I am researching about IMINIUM ION CYCLIZATION; CARBONYL METATHESIS; O-ALKYNYLANILINES; CONSTRUCTION; BASICITY; HETEROCYCLES; ALDEHYDES; INDOLINE; RULES; WATER, Saw an article supported by the . Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Amemiya, S; Okemoto, S; Tsubouchi, A; Saito, A. The CAS is 99-61-6. Through research, I have a further understanding and discovery of 3-Nitrobenzaldehyde

We developed a synthetic method for alpha-(aminoethyl)-alpha,beta-enones from aryl-substituted homopropargyl sulfonamides and aldehydes, representing the first synthesis of conjugated enones via alkyne aza-Prins cyclization. These products could be converted into pyrrolidines by a formal 5-endo-trig cyclization.

About 3-Nitrobenzaldehyde, If you have any questions, you can contact Amemiya, S; Okemoto, S; Tsubouchi, A; Saito, A or concate me.. Recommanded Product: 99-61-6

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

In 2019 J ENZYM INHIB MED CH published article about DIKETO ACID-DERIVATIVES; INTERFERENCE COMPOUNDS PAINS; DRUG-RESISTANCE MUTATIONS; REVERSE-TRANSCRIPTASE; RNASE-H; ACTIVE-SITE; DUAL INHIBITORS; MOLECULAR MECHANICS; COLORIMETRIC ASSAY; RNA/DNA HYBRID in [Massari, Serena; Desantis, Jenny; Sabatini, Stefano; Manfroni, Giuseppe; Felicetti, Tommaso; Cecchetti, Violetta; Tabarrini, Oriana] Univ Perugia, Dept Pharmaceut Sci, I-06123 Perugia, Italy; [Corona, Angela; Distinto, Simona; Caredda, Alessia; Maccioni, Elias; Tramontano, Enzo] Univ Cagliari, Dept Life & Environm Sci, Cittadella Univ Monserrato, I-09042 Cagliari, Italy; [Desantis, Jenny] Univ Perugia, Dept Chem Biol & Biotechnol, Perugia, Italy; [Pannecouque, Christophe] Katholieke Univ Leuven, Lab Virol & Chemotherapy, Rega Inst Med Res, Leuven, Belgium; [Tramontano, Enzo] CNR, Ist Ric Genet & Biomed, Monserrato, Italy in 2019, Cited 75. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Formula: C7H8N2O

The paper focussed on a step-by-step structural modification of a cycloheptathiophene-3-carboxamide derivative recently identified by us as reverse transcriptase (RT)-associated ribonuclease H (RNase H) inhibitor. In particular, its conversion to a 2-aryl-cycloheptathienoozaxinone derivative and the successive thorough exploration of both 2-aromatic and cycloheptathieno moieties led to identify oxazinone-based compounds as new anti-RNase H chemotypes. The presence of the catechol moiety at the C-2 position of the scaffold emerged as critical to achieve potent anti-RNase H activity, which also encompassed anti-RNA dependent DNA polymerase (RDDP) activity for the tricyclic derivatives. Benzothienooxazinone derivative 22 resulted the most potent dual inhibitor exhibiting IC(50)s of 0.53 and 2.90 mu M against the RNase H and RDDP functions. Mutagenesis and docking studies suggested that compound 22 binds two allosteric pockets within the RT, one located between the RNase H active site and the primer grip region and the other close to the DNA polymerase catalytic centre. [GRAPHICS] .

Formula: C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Massari, S; Corona, A; Distinto, S; Desantis, J; Caredda, A; Sabatini, S; Manfroni, G; Felicetti, T; Cecchetti, V; Pannecouque, C; Maccioni, E; Tramontano, E; Tabarrini, O or concate me.

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

In 2021 COLLOID SURFACE A published article about ONE-POT SYNTHESIS; IONIC LIQUID; EFFICIENT NANOCATALYST; SHELL MICROSPHERES; SILICA MATERIALS; MOLECULAR-SIEVE; CATALYST; CORE; NANOPARTICLES; NANOCOMPOSITES in [Shaker, Masoumeh; Elhamifar, Dawood] Univ Yasuj, Dept Chem, Yasuj 7591874831, Iran in 2021, Cited 107. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6. Application In Synthesis of 3-Nitrobenzaldehyde

In this study, preparation, characterization and catalytic application of a novel core-shell structured magnetic Tiloaded phenylene-based nanoporous organosilica (Mag@Ti-NOS) nanocomposite are developed. The Mag@TiNOS was synthesized via cetyltrimethylammonium bromide (CTAB) directed co-condensation of tetramethoxysilane (TMOS), tetrabutyl orthotitanate (TBOT) and 1,4-bis(triethoxysilyl)benzene (BTEB) over Mag@ SiO2 under alkaline conditions. This nanocomposite was characterized by using FT-IR, EDX, PXRD, VSM, SEM, TEM, XPS, ICP and TGA techniques. These analyses showed a core-shell structure with high chemical and thermal stability for the designed material. The Mag@Ti-NOS nanocomposite was employed as an effective, powerful and recyclable catalyst in the synthesis of tetrahydrobenzo[b]pyrans in H2O at 50 degrees C under ultrasonic conditions. This catalyst was recovered and reused several times without significant decrease in efficiency and stability. The recovered catalyst was analyzed by FT-IR, PXRD and SEM to study its stability during reaction process.

About 3-Nitrobenzaldehyde, If you have any questions, you can contact Shaker, M; Elhamifar, D or concate me.. Application In Synthesis of 3-Nitrobenzaldehyde

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

In 2021.0 SUGAR TECH published article about DEGRADATION; DIURON; HEXAZINONE; PESTICIDES; DISSIPATION; METRIBUZIN; FATE; VINASSE; CANE in [Viti, Marcela Lembi; dos Reis, Fabricia Cristina; Tornisielo, Valdemar Luiz] Univ Sao Paulo, Ctr Nucl Energy Agr, Piracicaba, SP, Brazil; [Mendes, Kassio Ferreira] Univ Fed Vicosa, Vicosa, MG, Brazil; [Dias Guimaraes, Ana Carolina] Univ Mato Grosso State, Alta Floresta, Mato Grosso, Brazil; [Martinez Soria, Maria Teresa] Univ La Rioja, Logrono, La Rioja, Spain in 2021.0, Cited 47.0. The Name is 1-Phenylurea. Through research, I have a further understanding and discovery of 64-10-8. Recommanded Product: 1-Phenylurea

This study evaluated the remobilization, mineralization, and metabolism of herbicide-bound residues in soils amended with various types of sugarcane waste. Soil with bound residues of three herbicides and fresh soil samples were added to the biometric flasks, followed by the addition of vinasse, filter cake, or sugarcane straw in order to reactivate the microbial activity. In sandy loam soil, higher mineralization was observed where filter cake was added, and the maximum mineralized percentage was 7.7, 46.7, and 8.1% of diuron-, hexazinone-, and metribuzin-bound residues, respectively. Conversely, this soil presented a greater percentage of re-extractable hexazinone and metribuzin residues when vinasse was added. Among the examined herbicides, a higher percentage of bound metribuzin residues remained in the soil (57.5-75.6%). It was possible to identify both metabolites and parent compounds in the re-extracted residues, implying either species could bind to the soil. Therefore, this study has shown that bound residues of three herbicides and their metabolites can become bioavailable, and mineralized or returned to the soil solution, which could adversely affect subsequent crops or non-target organisms. Hence, the remobilization of bound residues must be taken into account when assessing the environmental risk of herbicides in soils in registration processes.

About 1-Phenylurea, If you have any questions, you can contact Viti, ML; Mendes, KF; dos Reis, FC; Guimaraes, ACD; Soria, MTM; Tornisielo, VL or concate me.. Recommanded Product: 1-Phenylurea

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

Product Details of 64-10-8. In 2020.0 GENOME BIOL EVOL published article about 2,4-DICHLOROPHENOXYACETIC ACID; NUCLEOTIDE-SEQUENCE; INCP-1-BETA PLASMIDS; BACTERIAL CONSORTIUM; METABOLIC PATHWAY; DEGRADATION; RESISTANCE; TRANSPOSON; DIVERSITY; EVOLUTION in [Ozturk, Basak] Leibniz Inst DSMZ, German Collect Microorganisms & Cell Cultures, Jr Res Grp Microbial Biotechnol, Braunschweig, Germany; [Ozturk, Basak; Springael, Dirk] Katholieke Univ Leuven, Div Soil & Water Management, Leuven, Belgium; [Werner, Johannes] Leibniz Inst Baltic Sea Res, Dept Biol Oceanog, Rostock, Germany; [Meier-Kolthoff, Jan P.; Bunk, Boyke; Sproer, Cathrin] Leibniz Inst DSMZ, Dept Bioinformat & Databases, German Collect Microorganisms & Cell Cultures, Braunschweig, Germany in 2020.0, Cited 84.0. The Name is 1-Phenylurea. Through research, I have a further understanding and discovery of 64-10-8.

Biodegradation of the phenylurea herbicide linuron appears a specialization within a specific Glade of the Variovorax genus. The linuron catabolic ability is likely acquired by horizontal gene transfer but the mechanisms involved are not known. The full-genome sequences of six linuron-degrading Variovorax strains isolated from geographically distant locations were analyzed to acquire insight into the mechanisms of genetic adaptation toward linuron metabolism. Whole-genome sequence analysis confirmed the phylogenetic position of the linuron degraders in a separate Glade within Variovorax and indicated that they unlikely originate from a common ancestral linuron degrader. The linuron degraders differentiated from Variovorax strains that do not degrade linuron by the presence of multiple plasmids of 20-839 kb, including plasmids of unknown plasmid groups. The linuron catabolic gene clusters showed 1) high conservation and synteny and 2) strain-dependent distribution among the different plasmids. Most of them were bordered by IS1071 elements forming composite transposon structures, often in a multimeric array configuration, appointing IS1071 as a key element in the recruitment of linuron catabolic genes in Variovorax. Most of the strains carried at least one (catabolic) broad host range plasmid that might have been a second instrument for catabolic gene acquisition. We conclude that Glade 1 Variovorax strains, despite their different geographical origin, made use of a limited genetic repertoire regarding both catabolic functions and vehicles to acquire linuron biodegradation.

Product Details of 64-10-8. About 1-Phenylurea, If you have any questions, you can contact Ozturk, B; Werner, J; Meier-Kolthoff, JP; Bunk, B; Sproer, C; Springael, D or concate me.

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

I found the field of Plant Sciences; Chemistry; Pharmacology & Pharmacy very interesting. Saw the article Bioactive naphthoquinone and anthrone derivatives from endophytic Micromonospora sp. NEAU-gq13 published in 2019. Category: thiomorpholine, Reprint Addresses Wang, JD (corresponding author), Zhejiang Hisun Pharmaceut Co Ltd, Zhejiang Key Lab Antifungal Drugs, Taizhou 318000, Peoples R China.; Xiang, WS (corresponding author), Northeast Agr Univ, Sch Life Sci, Life Sci & Biotechnol Res Ctr, Harbin 150030, Heilongjiang, Peoples R China.. The CAS is 90-44-8. Through research, I have a further understanding and discovery of Anthrone

Two new naphthalenone derivatives, 5-hydroxy-4-oxo-2-(2-oxopropyl)-1,2,3,4-tetrahydronaphthalen-1-yl acetate (1) and 5-hydroxy-2-(2-hydroxypropyl)naphthalene-1,4-dione (2), together with two new anthrone derivatives, (S)-2,5-dihydroxy-2-methyl-1,2,3,4-tetrahydroanthracene-9,10-dione (3) and 4,5-dihydroxy-2-methyl-9H-xanthen-9-one (4), were isolated from the fermentation broth of endophytic Micromonospora sp. NEAU-gq13. Their structures were determined by 1D-NMR, 2D-NMR, and HR-ESI-MS analysis. Compounds 2 and 3 exhibited strong cytotoxic activity against human central nervous system cancer (SF-268) with the IC50 values of 3.04 and 5.66 mu g/ml, respectively. Moreover, compound 2 also displayed potent activity against human liver cancer (HepG2) with an IC50 value of 1.01 mu g/ml.

About Anthrone, If you have any questions, you can contact Li, JS; Zhang, H; Qi, H; Wang, JD; Xiang, WS or concate me.. Category: thiomorpholine

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

Authors Ram, S; Shaifali; Chauhan, AS; Sheetal; Sharma, AK; Das, P in WILEY-V C H VERLAG GMBH published article about CATALYZED OXIDATIVE SYNTHESIS; CASCADE SYNTHESIS; O-AMINOBENZAMIDES; N-HETEROCYCLES; LUOTONIN-A; QUINAZOLIN-4(3H)-ONES; DERIVATIVES; CYCLIZATION in [Ram, Shankar; Shaifali; Chauhan, Arvind Singh; Sheetal; Sharma, Ajay Kumar; Das, Pralay] CSIR Inst Himalayan Bioresource Technol, Nat Prod Chem & Proc Dev Div, Palampur 176061, Himachal Prades, India; [Ram, Shankar; Shaifali; Chauhan, Arvind Singh; Sheetal; Sharma, Ajay Kumar; Das, Pralay] CSIR IHBT, Acad Sci & Innovat Res, Palampur 176061, Himachal Prades, India in 2019, Cited 53. Recommanded Product: 88-68-6. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

An efficient and convenient strategy for the synthesis of diversely substituted quinazolinones from o-carbamoyl/cyano aniline and aryl iodides using oxalic acid as a CO source under polystyrene supported palladium (Pd@PS) nanoparticles (NPs) catalyzed conditions has been developed. In this study, oxalic acid has been employed as safe, economic, environmentally benign, sustainable and bench-stable, solid CO surrogate under Double-Layer-Vial (DLV) system for the synthesis of 2-aryl quinazolinones. This methodology does not require any special high-pressure equipment like autoclaves, microwaves, etc. Moreover, a simple procedure for catalyst preparation, catalyst recyclability, easy handling of reaction, additive and base-free generation of CO, excellent to good yields and vast substrate scope are the additional features of developed protocol.

Recommanded Product: 88-68-6. About 2-Aminobenzamide, If you have any questions, you can contact Ram, S; Shaifali; Chauhan, AS; Sheetal; Sharma, AK; Das, P or concate me.

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

COA of Formula: C7H5NO3. Authors Khoshdel, MA; Shirini, F; Langarudi, MSN; Zabihzadeh, M; Biglari, M in ROYAL SOC CHEMISTRY published article about in [Alipour Khoshdel, Meysam; Shirini, Farhad; Nikoo Langarudi, Mohaddeseh Safarpoor; Zabihzadeh, Mehdi; Biglari, Mohammad] Univ Guilan, Dept Chem, Coll Sci, Rasht 4133519141, Iran in 2021.0, Cited 44.0. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

The development of environmentally benign synthetic protocols has attracted increasing attention in recent organic syntheses. As a part of this concept, our group synthesized a new natural deep eutectic solvent (NADES) by using gabapentin and choline chloride. After characterization by FTIR, H-1 and C-13 NMR, and mass spectra, the prepared NADES was utilized as an efficacious catalyst for the synthesis of 4H-pyran scaffolds such as tetrahydrobenzo[b]pyran and pyrano[2,3-d]pyrimidinone(thione) derivatives. The use of inexpensive and bio-compatible reagents for the synthesis of the catalyst, a simple and green procedure for the preparation of the catalyst and products, short reaction times, high yields of the products, and applicability to large-scale synthesis are the prominent features of this protocol. Also, the catalyst could be recovered easily and recycled up to five times without significant loss of its catalytic activity.

About 3-Nitrobenzaldehyde, If you have any questions, you can contact Khoshdel, MA; Shirini, F; Langarudi, MSN; Zabihzadeh, M; Biglari, M or concate me.. COA of Formula: C7H5NO3

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

An article Aerobic oxidative synthesis of quinazolinones and benzothiazoles in the presence of laccase/DDQ as a bioinspired cooperative catalytic system under mild conditions WOS:000528043700039 published article about ONE-POT SYNTHESIS; HETEROGENEOUS CATALYST; SELECTIVE OXIDATION; C-H; EFFICIENT; DDQ; DERIVATIVES; ALCOHOLS; GREEN; 2-ARYLBENZOTHIAZOLES in [Ghorashi, Nadia; Shokri, Zahra; Moradi, Reza; Rostami, Amin] Univ Kurdistan, Fac Sci, Dept Chem, Sanandaj 6617715175, Iran; [Abdelrasoul, Amira; Rostami, Amin] Univ Saskatchewan, Dept Chem & Biol Engn, 57 Campus Dr, Saskatoon, SK S7N 5A9, Canada in 2020, Cited 53. Recommanded Product: 2-Aminobenzamide. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

The current study applied laccase/DDQ as a bioinspired cooperative catalytic system for the synthesis of quinazolinones (80-95% yield) and benzothiazoles (65-98% yield) using air or O-2 as ideal oxidants in aqueous media at ambient temperature. The aerobic oxidative cyclization reactions occur in two steps: (i) chemical cyclization; (ii) chemoenzymatic oxidation. These methods are more environment-friendly, efficient, simple and practical than other reported methods due to the use of O-2 as an oxidant, laccase as an eco-friendly biocatalyst, aqueous media as the solvent and free from any toxic transition metal and halide catalysts. Therefore, these methods can be applied in pharmaceutical and other sensitive synthetic procedures.

About 2-Aminobenzamide, If you have any questions, you can contact Ghorashi, N; Shokri, Z; Moradi, R; Abdelrasoul, A; Rostami, A or concate me.. Recommanded Product: 2-Aminobenzamide

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