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N-[2-(4-methoxy-phenyl)-5-(3-nitro-benzylidene)-4-oxothiazolidin-3-yl]biphenyl-4-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1320356-65-7

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1320356-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1320356-65-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,0,3,5 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1320356-65:
(9*1)+(8*3)+(7*2)+(6*0)+(5*3)+(4*5)+(3*6)+(2*6)+(1*5)=117
117 % 10 = 7
So 1320356-65-7 is a valid CAS Registry Number.

1320356-65-7Downstream Products

1320356-65-7Relevant academic research and scientific papers

Synthesis of 2-(aryl)-5-(arylidene)-4-thiazolidinone derivatives with potential analgesic and anti-inflammatory activity

Deep, Aakash,Jain, Sandeep,Sharma, Prabodh Chander,Phogat, Priyanka,Malhotra, Manav

, p. 1652 - 1659 (2012)

A series of novel N-[5-(arylidene)-2-(aryl)-4-oxo-thiazolidin-3-yl]-4- biphenylcarboxamide derivatives was synthesized and evaluated for analgesic and anti-inflammatory activity. In this study, biphenyl-4-carboxylic acid hydrazide was converted to the corresponding aryl hydrazones using aryl aldehydes in the presence of catalytic amount of glacial acetic acid. The aryl hydrazones on reaction with thioglycolic acid in the presence of anhydrous zinc chloride yielded N-[2-(aryl)-4-oxo-thiazolidin-3-yl]-4-biphenylcarboxamide which further on reaction with aromatic aldehydes in the presence of anhydrous sodium acetate and glacial acetic acid furnished the title compounds. All compound exhibited anti-inflammatory activity at the dose 10 mg/kg. The structures of all these newly synthesized compounds were confirmed by their elemental analyses (C, H, N) and spectral data (IR and 1H NMR). Springer Science+Business Media, LLC 2011.

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