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3-amino-5-(phenylamino)-1,2-thiazole-4-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

117377-43-2

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117377-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117377-43-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,3,7 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 117377-43:
(8*1)+(7*1)+(6*7)+(5*3)+(4*7)+(3*7)+(2*4)+(1*3)=132
132 % 10 = 2
So 117377-43-2 is a valid CAS Registry Number.

117377-43-2Relevant academic research and scientific papers

Synthesis and antiproliferative assessments of new derivatives of isothiazolo[3,4-d]pyrimidine

Khoshniazi, Hamideh,Eshghi, Hossein,Tayarani-Najjaran, Mona,Tayarani-Najaran, Zahra,Saadat, Kayvan,Shiri, Ali

, p. 193 - 201 (2020/11/12)

Various derivatives of 5-aryl-4-imino-3-(phenylamino)-4,5-dihydroisothiazolo[3,4-d]pyrimidines (3a-f) were synthesized. The synthesis has been done through treatment of 3-amino-4-cyano-5-(phenylamino)isothiazole with various aryl isothiocyanates. The isothiazole skeleton was obtained by the reaction of malononitrile and phenyl isothiocyanate followed by chloramine treatment. Some of the synthesized dihydroisothiazolo[3,4-d]pyrimidines were tested against different cancer cell lines, including ACHN, HeLa, HL-60, MCF-7, and PC3. Malignant cells were cultured in RPMI medium and incubated with different concentrations of the mentioned compounds. Cell viability was assessed using the MTS assay. The cytotoxicities of the synthesized compounds are not significant and are probably safe for other biological use.

Heterocyclic compounds and uses thereof

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Page/Page column 10, (2008/06/13)

Substituted isothiazole compounds and compositions are provided, wherein particularly preferred compositions and methods are directed towards inhibition of various protein kinases (especially MEK and/or ERK). Consequently, particularly preferred methods i

A Facile Synthesis of 3-Amino-5-substitutedaminoisothiazole-4-carboxylic Acid Derivatives

Shishoo, C. J.,Devani, M. B.,Ananthan, S.,Bhadti, V. S.,Ullas, G. V.

, p. 759 - 765 (2007/10/02)

A facile, general and one-pot method for the preparation of 3-amino-5-substituted-aminoisothiazole-4-carboxylic acid derivatives, in high yields, by the aminative cyclization of 3-amino-3-mercaptoacrylonitriles is described.

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