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ethyl 3-amino-4-(4-chlorophenyl)-6-(2-thienyl)thieno[2,3-b]pyridine-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

296797-45-0

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296797-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 296797-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,6,7,9 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 296797-45:
(8*2)+(7*9)+(6*6)+(5*7)+(4*9)+(3*7)+(2*4)+(1*5)=220
220 % 10 = 0
So 296797-45-0 is a valid CAS Registry Number.

296797-45-0Relevant academic research and scientific papers

Synthesis and reactions of some pyridopyrimidine and thienopyridine derivatives for antiviral evaluation

Yousif,Morsy,Sayed

experimental part, p. 651 - 660 (2010/10/18)

COMPOUNDS 6-amino-4-(4-chlorophenyl)-2-thien-2-ylpyridine5-carbonitrile (2) and 4-(4-chlorophenyl)-6-thioxo-2-thien-2-yll,6-dihydropyridine-5-carbonitrile (9) were prepaied using 3-(4-chlorophenyl)-l-thien-2-ylpropenone (I) and malononitrile or cyanothioacetamide, respectively. Pyridine derivative 2 was in turn used as a precursor for preparation of some pyridopyrimidine and fused pyridopyrimidine derivatives 3-8. On the other hand, the pyridine derivative 9 was used in preparation of thienopyridine derivatives 10 and 11. Moreover, fusion of compound 11 with excess of benzoyl chloride ' afforded 4-(4-chlorophenyl)-2-phenyl-7-thien-2-yl-3H-pyrido [3′,2′:4,5] thieno[3,2-d] pyrimidin-4-one (12).

Synthesis and reactions of some new heterocyclic compounds containing the thienylthieno[2,3-b]pyridine moiety

Bakhite, Etify A.,Abdel-Rahman, Abdu E.,Mohamed, Omima S.,Thabet, Eman A.

, p. 1983 - 2006 (2007/10/03)

(4-Aryl-3-cyano-6-(2-thienyl)pyridin-2-ylthio)acethydrazides (5a-c), 3-amino-4-aryl-6-(2-thienyl)thieno[2,3-b]pyridine-2-carbohydrazides (6a-c) and 3-amino-4-phenyl-6-(2-thienyl)thieno[2,3-b]pyridine-2-carboxylic acid (30) were prepared and employed as key intermediates in the synthesis of the title compounds.

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