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5-methyl-2-(phenylamino)thiazol-4(5H)-one is a chemical compound with the molecular formula C10H9N3OS. It is a derivative of the thiazolone class of heterocyclic compounds, characterized by the presence of a sulfur atom and a nitrogen atom in the ring structure. This particular compound features a methyl group at the 5-position, a phenylamino group at the 2-position, and a carbonyl group at the 4-position. It is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the preparation of other organic compounds. The compound's structure and properties make it a versatile building block in organic synthesis, with potential applications in the development of new drugs and other chemical products.

4695-20-9

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4695-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4695-20-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,9 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4695-20:
(6*4)+(5*6)+(4*9)+(3*5)+(2*2)+(1*0)=109
109 % 10 = 9
So 4695-20-9 is a valid CAS Registry Number.

4695-20-9Relevant academic research and scientific papers

Synthesis of thiazolidin-4-ones via [3+2] cycloaddition of in situ generated aza-oxyallylic cations with isothiocyanates

Wang, Gangqiang,Zhao, Sen,Chen, Rongxing,Yang, Liangfeng,Wang, Jian,Guo, Haibing,Wu, Minghu,Domena, Justin,Xing, Yalan,Sun, Shaofa

, p. 4308 - 4311 (2017)

A highly efficient one-pot synthesis of thiazolidin-4-ones via [3+2] cycloaddition of aza-oxyallylic cations with isothiocyanates is developed. The aza-oxyallyic cations were generated in situ in the present of a base. This cycloaddition reaction allows t

New methods for the synthesis of 2-aminothiazolones

Caille, Seb,Bercot, Eric A.,Cui, Sheng,Faul, Margaret M.

, p. 2003 - 2006 (2008/09/20)

(Chemical Equation Presented) Two new methods for the synthesis of 2-aminothiazolones from 2-(4-methoxybenzylthio)acetic acids are described. A single reagent and simple experimental conditions are used in the key tandem deprotection-cyclization process. In the first approach 2-aminothiazolones are directly accessed via cyclization of the corresponding N-acylisothioureas. The second complementary approach provides access to a variety of 2-thiomethylthiazolones via cyclization of N-acyldithioimidates. The product 2-thiomethylthiazolones are then efficiently converted to 2-aminothiazolones via amine displacement.

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