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Mercapto-3-(p-tolyl)acrylic acid, also known as 3-(4-methylphenylthio)acrylic acid, is an organic compound characterized by the presence of a mercapto (-SH) group and a p-tolyl (4-methylphenyl) group. This colorless crystalline solid has a molecular formula of C9H8O2S and a molecular weight of 176.22 g/mol. It is a derivative of acrylic acid, with a sulfur-containing functional group that imparts unique chemical properties. The compound is used in various applications, including the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its reactivity, due to the presence of the mercapto group, allows for the formation of disulfide bonds and other sulfur-containing linkages, which are important in the development of certain drugs and chemical compounds.

5765-79-7

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5765-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5765-79-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,6 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5765-79:
(6*5)+(5*7)+(4*6)+(3*5)+(2*7)+(1*9)=127
127 % 10 = 7
So 5765-79-7 is a valid CAS Registry Number.

5765-79-7Relevant academic research and scientific papers

Structure activity relationship studies on rhodanines and derived enethiol inhibitors of metallo-β-lactamases

Zhang, Dong,Markoulides, Marios S.,Stepanovs, Dmitrijs,Rydzik, Anna M.,El-Hussein, Ahmed,Bon, Corentin,Kamps, Jos J.A.G.,Umland, Klaus-Daniel,Collins, Patrick M.,Cahill, Samuel T.,Wang, David Y.,von Delft, Frank,Brem, Jürgen,McDonough, Michael A.,Schofield, Christopher J.

, p. 2928 - 2936 (2018)

Metallo-β-lactamases (MBLs) enable bacterial resistance to almost all classes of β-lactam antibiotics. We report studies on enethiol containing MBL inhibitors, which were prepared by rhodanine hydrolysis. The enethiols inhibit MBLs from different subclasses. Crystallographic analyses reveal that the enethiol sulphur displaces the di-Zn(II) ion bridging ‘hydrolytic’ water. In some, but not all, cases biophysical analyses provide evidence that rhodanine/enethiol inhibition involves formation of a ternary MBL enethiol rhodanine complex. The results demonstrate how low molecular weight active site Zn(II) chelating compounds can inhibit a range of clinically relevant MBLs and provide additional evidence for the potential of rhodanines to be hydrolysed to potent inhibitors of MBL protein fold and, maybe, other metallo-enzymes, perhaps contributing to the complex biological effects of rhodanines. The results imply that any medicinal chemistry studies employing rhodanines (and related scaffolds) as inhibitors should as a matter of course include testing of their hydrolysis products.

POTASSIUM FLUORIDE ON ALUMINA: CONDENSATION OF 3-METHYL-2-THIONO-4-THIAZOLIDINONE WITH ALDEHYDES. SYNTHESIS OF α-THIOACRYLIC ACIDS AND PHOSPHONOTHIONOTHIAZOLIDINONES

Villemin, Didier,Alloum, Abdelkrim Ben

, p. 33 - 42 (2007/10/02)

3-Methyl-2-thiono-4-thiazolidinone and aromatic aldehydes adsorbed on potassium fluoride on alumina gave under microwave irradiation 5-arylidene-3-methyl-2-thiono-4-thiazolidinones in 70percent to 90percent yield.These compounds can be cleaved with sodium

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