Day: July 20, 2021

You could be based in a university, combining chemical research with teaching; or in a public-sector research center, helping to ensure national healthcare provision keeps pace with new discoveries. In an article, author is Sreerama, Rakesh, once mentioned the application of 93-07-2, Name is 3,4-Dimethoxybenzoic acid, molecular formula is C9H10O4, molecular weight is 182.1733, MDL number is MFCD00002500, category is thiomorpholine. Now introduce a scientific discovery about this category, Category: thiomorpholine.

A one-pot procedure for the synthesis of novel 1,2,3-triazole derivatives (5a-5l) in good yields (63 to 77%) using different sulfonic acids and 4-(prop-2-yn-1-yl)thiomorpholine 1,1-dioxide through the in situ generated sulfonyl azides was developed. The structures of the newly synthesized compounds were confirmed by H-1 NMR, C-13 NMR, mass spectrometry, and elemental analysis. The newly synthesized compounds were screened for in vitro antibacterial activity and free radical scavenging activity in terms of hydrogen donating or radical scavenging ability by the DPPH method. Among all, the compound N-(4-((4-((1,1-dioxidothiomorpholino) methyl)-1H-1,2,3-triazol-1-yl)sulfonyl)phenyl) acetamide (5l) was found to exhibit potent activity as compared to the standard drugs.

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

Academic researchers, R&D teams, teachers, students, policy makers and the media all rely on us to share knowledge that is reliable, accurate and cutting-edge. In an article, author is REDDY, DB, once mentioned the application of 83-56-7, Name is Naphthalene-1,5-diol, molecular formula is C10H8O2, molecular weight is 160.17, MDL number is MFCD00003980, category is thiomorpholine. Now introduce a scientific discovery about this category, Recommanded Product: Naphthalene-1,5-diol.

A series of new 2-aroyl-3, 5-diaryltetrahydro-1, 4- thiazine-1, 1-dioxides (2) has been synthesized either from phenacylsulfonylacetic acids (1) or phenacylstyryl sulfones (3), which in turn are obtained from the substituted acetophenones or styrenes, respectively. Another series of alkoxycarbonyl-3-aryl-5(4-methyl-phenyl)tetrahydro-l, 4-thiazine-1, 1-dioxides (5) has been prepared from Z (or E)-alkyl 4-methylstyrylsulfonyl acetates (4). The desired 4 has been obtained from the corresponding acetylenes or 4-methylstyrene. The structures of 2 and 5 and their preferred chair conformations have been deduced by the analysis of high resolution NMR data supported by correlation spectroscopy.

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

Academic researchers, R&D teams, teachers, students, policy makers and the media all rely on us to share knowledge that is reliable, accurate and cutting-edge. In an article, author is Levin, JI, once mentioned the application of 3695-77-0, Name is Triphenylmethanethiol, molecular formula is C19H16S, molecular weight is 276.3953, MDL number is MFCD00004854, category is thiomorpholine. Now introduce a scientific discovery about this category, Reference of 3695-77-0.

A series of thiomorpholine sulfonamide hydroxamate TACE inhibitors, all bearing propargylic ether P1′ groups, was explored. In particular, compound 5h has excellent in vitro potency against isolated TACE enzyme and in cells, oral activity in a model of TNF-alpha production and a collagen-induced arthritis model, was selected as a clinical candidate for the treatment of RA. (C) 2005 Elsevier Ltd. All rights reserved.

Reference of 3695-77-0, You can get involved in discussing the latest developments in this exciting area about 3695-77-0.

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

Quality Control of 2-Bromo-4′-chloro-1,1′-biphenyl, Chemistry graduates have much scope to use their knowledge in a range of research sectors, including roles within chemical engineering, chemical and related industries, healthcare and more.179526-95-5, Name is 2-Bromo-4′-chloro-1,1′-biphenyl, SMILES is ClC1=CC=C(C2=CC=CC=C2Br)C=C1, belongs to thiomorpholine compound. In a article, author is Krishnaraj, Thulasiraman, introduce new discover of the category.

Treatment of 2-(2-oxo-2-arylethylthio)-N-(4H-1,2,4-triazol-3-yl)acetamides with paraformaldehyde in the presence of a base has led to a tandem chemoselective hydroxymethylation followed by cyclization yielding a set of novel 6-aroyl-4-(4H-triazol-3-yl)thiomorpholin-3-ones. The thiomorpholine ring has been found to have a boat like conformation in these compounds as evidenced by NOESY NMR spectrum. (C) 2011 Elsevier Ltd. All rights reserved.

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

New research progress on 529-35-1 in 2021. Chemical research careers are more diverse than they might first appear, as there are many different reasons to conduct research and many possible environments. 529-35-1, Name is 5,6,7,8-Tetrahydro-1-naphthol, molecular formurla is C10H12O. In a document, author is Morkved, EH, introducing its new discovery. Recommanded Product: 5,6,7,8-Tetrahydro-1-naphthol.

Nickel(II) octa(4-morpholinyl)- (11a) and copper(II) octa(l-pyrrolidinyl)- (11b) azaphthalocyanines have been prepared from the corresponding pyrazine diiminoimides (10). The precursor pyrazine dicarbonitriles (2) gave 6-cyanopyrazine-5-alkyl carboximidates (3-9) as stable intermediates when reacted with ammonia and catalytic amounts of sodium alkoxide in alcohols. Compounds 3-9 were converted to the diiminoimides 10 upon reflux in propanol or butanol for several hours. This unusual reaction pattern was observed for pyrazine-2,3-dicarbonitriles 2 substituted in the 5- and B-positions with morpholine, thiomorpholine, piperidine or pyrrolidine. Copyright (C) 1999 John Wiley & Sons, Ltd.

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

In chemical reaction engineering, simulations are useful for investigating and optimizing a particular reaction process or system. In an article, author is Barbachyn, MR, once mentioned the application of 1965-09-9, Name is 4,4-Oxydiphenol, molecular formula is C12H10O3, molecular weight is 202.206, MDL number is MFCD00016463, category is thiomorpholine. Now introduce a scientific discovery about this category, Product Details of 1965-09-9.

During the course of our investigations in the oxazolidinone antibacterial agent area, we have identified a subclass with especially potent in vitro activity against mycobacteria. The salient structural feature of these oxazolidinone analogues, 6 (U-100480), 7 (U-101603), and 8 (U-101244), is their appended thiomorpholine moiety. The rational design, synthesis, and evaluation of the in vitro antimycobacterial activity of these analogues is described. Potent activity against a screening strain of Mycobacterium tuberculosis was demonstrated by 6 and 7 (minimum inhibitory concentrations or MIC’s less than or equal to 0.125 mu g/mL). Oxazolidinones 6 and 8 exhibit MIC(90) values of 0.50 mu g/mL or less against a panel of organisms consisting of five drug-sensitive and five multidrug-resistant strains of M. tuberculosis, with 6 being the most active congener. Potent in vitro activity against other mycobacterial species was also demonstrated by 6. For example, 6 exhibited excellent in vitro activity against multiple clinical isolates of Mycobacterium avium complex (MIC’s = 0.5-4 mu g/mL). Orally administered 6 displays in vivo efficacy against M. tuberculosis and M. avium similar to that of clinical comparators isoniazid and azithromycin, respectively. Consideration of these factors, along with a favorable pharmacokinetic and chronic toxicity profile in rats, suggests that 6 (U-100480) is a promising antimycobacterial agent.

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

You could be based in a university, combining chemical research with teaching; or in a public-sector research center, helping to ensure national healthcare provision keeps pace with new discoveries. In an article, author is Battula, Kumara Swamy, once mentioned the application of 126534-31-4, Name is (S)-alpha-(Chloromethyl)-2,4-dichlorobenzyl alcohol, molecular formula is C8H7Cl3O, molecular weight is 225.4996, MDL number is MFCD07776655, category is thiomorpholine. Now introduce a scientific discovery about this category, SDS of cas: 126534-31-4.

In this report, we describe the synthesis and biological evaluation of a new series of (4-((1-(aryl)-1H-1,2,3-triazol-4-yl) methoxy) phenyl)(1,1-dioxidothiomorpholino) methanone derivatives (6a-6n). All the new derivatives were well analyzed by (HNMR)-H-1, (CNMR)-C-13, FTIR, mass spectral and elemental data. The synthesized compounds were screened for in vitro anticancer activity against three cancer cell lines (MCF-7, HeLa, and HEK293) and compared with standard drug cisplatin. Three (6b, 6g and 6i) out of fourteen derivatives exhibited potent anticancer activity against MCF-7, HeLa, and HEK293. Two ( 6b and 6g) potent hybrids were screened for in vivo studies against EAC bearing mice and found to possess potential anticancer activity.

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

While the job of a research scientist varies, most chemistry careers in research are based in laboratories, where research is conducted by teams following scientific methods and standards., Electric Literature of 100-21-0, 100-21-0, Name is Terephthalic acid, molecular formula is C8H6O4, belongs to thiomorpholine compound. In a document, author is Battula, Kumaraswamy, introduce the new discover.

A convenient synthesis of novel 1,4-disubstituted 1,2,3-triazoles (4a-j and 5a-j) is reported via copper(I)-catalyzed one pot [3+ 2] cycloaddition of various alkyl halides, sodium azide with 4-(prop-2-yn-1-yl) thiomorpholine and 4-(prop-2-yn-1-yl) thiomorpholine 1,1-dioxide. All the synthesized compounds were investigated for their antimicrobial activity. Compounds 4a, 4b, 4c, 4g, 5a and 5j against Staphylococcus epidermidis, 4a, 5a and 5d against Pseudomonas aeruginosa, 4a, 4b and 4g against Klebsiella pneumoniae, 4b, 5a and 5d against S. aureus and 5b, 5e and 5j against Bacillus subtilis showed excellent antibacterial activity compared to the standard drugs penicillin and streptomycin. Compounds 4c, 4e, 4f, 4j, 5c, 5d, 5g and 5j registered moderate antifungal activity as compared with the standard drug amphotericin B.

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

As a society publisher, everything we do is to support the scientific community – so you can trust us to always act in your best interests, and get your work the international recognition that it deserves., Recommanded Product: 119-47-1, 119-47-1, Name is 2,2-Methylenebis(6-tert-butyl-p-cresol), molecular formula is C23H32O2, belongs to thiomorpholine compound. In a document, author is Starosta, Radoslaw, introduce the new discover.

Herein, a series of CuI or CuNCS complexes with neocuproine (2,9-dimethyl-1,10-phenanthroline: dmp) and two tris(aminomethyl)phosphines derived from morpholine (P(CH2N(CH2CH2)(2)O)(3)) or thiomorpholine (P(CH2N(CH2CH2)(2)S)(3)) were tested as cytotoxic agents in vitro towards mouse colon carcinoma (CT26) and human lung adenocarcinoma (A549). The studies showed that the complexes exhibit potential antitumor properties, displayed by IC50 values below 10m towards the tested cell lines, in the case of 4-h incubation time with the examined compounds. Moreover, a high antimicrobial activity of all the complexes was observed against Staphylococcus aureus and Candida albicans with minimal inhibitory concentrations equal to 1-2g/mL. To gain insight into the molecular mechanism of biological activity of the complexes, we investigated also their interactions with plasmid DNA (pUC18) and the human and bovine serum albumins. Gel electrophoresis experiments demonstrated that all the compounds were comparably efficient in DNA degradation process; however, luminescence quenching showed surprising dependence on the interactions strength of the used compounds with the albumins. Apart from exceptionally effective [CuI(dmp)P(CH2N(CH2CH2)(2)O)(3)], the complexes with P(CH2N(CH2CH2)(2)O)(3) quenched more strongly luminescence of bovine serum albumin, while the complexes with P(CH2N(CH2CH2)(2)S)(3) were more active in the quenching of human serum albumin luminescence.

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

Chemistry involves the study of all things chemical – chemical processes, chemical compositions and chemical manipulation – in order to better understand the way in which materials are structured, how they change and how they react in certain situations. , COA of Formula: https://www.ambeed.com/products/13680-35-8.html, 13680-35-8, Name is 4,4-Methylenebis(2,6-diethylaniline), molecular formula is C21H30N2, belongs to thiomorpholine compound. In a document, author is Amezcua, CA, introduce the new discover.

Thiomorpholine-N-borane was synthesized via amine displacement of BH3 from tetrahydrofuran-borane which had been prepared from NaBH4 and BF3. Et2O in tetrahydrofuran. Acid-catalyzed hydrolysis occurs only slightly faster than for morpholine-borane, the difference being attributed to a small difference in the electronic inductive effects of sulfur and oxygen in the 4-position of the respective adducts. Reaction with NaOCl exhibits a stoichiometric [OCl-]:[S(CH2)(4)NHBH3] ratio of 5:1. This is attributed to consumption of 3 mol of hypochlorite for the oxidation of hydridic hydrogen in BH3, one for the chlorination of nitrogen and another in attack at sulfur presumably resulting in sulfoxide formation. At pH 9.1-10.4, the initial reaction of hypochlorite with thiomorpholine-borane is several times faster than with morpholine-borane and, unlike the reaction with morpholine-borane, relatively insensitive to pH. Whereas hypochlorite oxidation of morpholine-borane has been proposed to occur primarily through reaction with HOCl, it is speculated that thiomorpholine-borane is also susceptible to attack by hypochlorite ion. (C) 1999 Elsevier Science S.A. All rights reserved.

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