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126106-28-3

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126106-28-3 Usage

General Description

2-(4-Hydroxy-1,3-thiazol-2-yl)ethanethioamide is a chemical compound that belongs to the thiazole family. It is a thioamide derivative with a thiazole ring containing a hydroxyl group, which gives it some unique properties. Thioamides are known for their diverse range of biological activities, and the presence of the thiazole ring in this compound suggests potential pharmaceutical or medicinal applications. The compound may have potential as a drug lead or pharmacological tool in research due to its structural features and the known biological activities of related compounds. Further research is needed to explore its potential uses and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 126106-28-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,1,0 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 126106-28:
(8*1)+(7*2)+(6*6)+(5*1)+(4*0)+(3*6)+(2*2)+(1*8)=93
93 % 10 = 3
So 126106-28-3 is a valid CAS Registry Number.

126106-28-3Relevant articles and documents

α-CYANOTHIOACETAMIDE IN HETEROCYCLIC SYNTHESIS: A NEW APPROACH FOR THE SYNTHESIS OF 4-OXO-4,5-DIHYDRO-1,3-THIAZOLE-2-THIOACETAMIDE DERIVATIVES

Abdelaziz, Mahfouz A..,El-Sharabasy, Salwa A.,Gawad, Soad M. Abdel

, p. 231 - 236 (2007/10/02)

Treatment of α-cyanothioacetamide (1) with thioglycolic acid in pyridine led to the formation of 4-oxo-4,5-dihydro-1,3-thiazole-2-thioacetamide (2). (2) reacted with two equivalents of aryldiazonium chloride to afford the diarylazo derivatives (3a-c).However, when (2) was reacted with an equivalent amount of aryldiazonium chloride the monoarylazo derivatives (4a-c) were obtained and not (5a-c), which can be prepared via the reaction of thioglycilic acid with α-arylazo-α-cyano-thioacetamide (6a-c).With aromatic aldehydes (2) reacted to give the diylidene derivatives (7a-d).The structures of the isolated products were established by elemental analyses, and spectral data studies.

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