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8-cyano-3-(4-fluorophenyl)-5-methyl-7-(methylthio)-2-(tertbutylamino)-pyrido[4,3-d]pyrimidin-4(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1097699-89-2

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1097699-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1097699-89-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,7,6,9 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1097699-89:
(9*1)+(8*0)+(7*9)+(6*7)+(5*6)+(4*9)+(3*9)+(2*8)+(1*9)=232
232 % 10 = 2
So 1097699-89-2 is a valid CAS Registry Number.

1097699-89-2Downstream Products

1097699-89-2Relevant academic research and scientific papers

A convenient synthesis and biological activity of novel pyrido[4,3-d]pyrimidin-4(3H)-ones

Ren, Qingyun,Xia, ShiYan,Gu, Yucheng,Li, Baoju,He, Hongwu

, p. 647 - 652 (2015/05/13)

Fifteen novel 2-alkylamino-3-aryl-8-cyano-5-methyl-7-(methylthio)-pyrido[4,3-d]pyrimidin-4(3H)-ones 6a, 6b, 6c, 6d, 6e, 6f, 6g, 6h, 6i, 6j, 6k, 6l, 6m, 6n, 6o were designed and have been successfully synthesized via tandem aza-Wittig and annulation reacti

A convenient synthesis and biological activity of novel pyrido[4,3-d]pyrimidin-4(3H)-ones

Ren, Qingyun,Shi, Yanxia,Gu, Yucheng,Li, Baoju,He, Hongwu

, p. 285 - 290 (2014/04/17)

Fifteen novel 2-alkylamino-3-aryl-8-cyano-5-methyl-7-(methylthio)-pyrido[4, 3-d]pyrimidin-4(3H)-ones 6a, 6b, 6c, 6d, 6e, 6f, 6g, 6h, 6i, 6j, 6k, 6l, 6m, 6n, 6o were designed and have been successfully synthesized via tandem aza-Wittig and annulation reactions with the corresponding iminophosphorances 4, aryl isocyanate, and amines in good yields. Their structures were clearly verified by IR, 1H NMR, EI-MS spectroscopy and elemental analysis, and in the case of compound 6i, analyzed by single-crystal X-ray diffraction further. The preliminary results of an in vivo bioassay showed that some compounds display moderate antifungal activity.

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