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2-{2-cyano-2-[4-(4-methoxy-benzylidene)-5-oxo-3-phenyl-thiazolidin-2-ylidene]-acetylamino}-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1224701-93-2

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1224701-93-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1224701-93-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,7,0 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1224701-93:
(9*1)+(8*2)+(7*2)+(6*4)+(5*7)+(4*0)+(3*1)+(2*9)+(1*3)=122
122 % 10 = 2
So 1224701-93-2 is a valid CAS Registry Number.

1224701-93-2Downstream Products

1224701-93-2Relevant academic research and scientific papers

Synthesis and antimicrobial activities of some new thiazole and pyrazole derivatives based on 4,5,6,7-tetrahydrobenzothiophene moiety

Gouda,Berghot,Abd El-Ghani, Ghada E.,Khalil

experimental part, p. 1338 - 1345 (2010/05/18)

2-(5-oxothiazolidinone)-cyanoacetamido derivative 3 was prepared in two steps by reaction of 2-(2-cyano-acetylamino)-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxamide (1) with phenyl isothiocyanate and chloroacetyl chloride, which diazocoupled with p-tolyldiazonium chloride in pyridine to afford the corresponding hydrazono derivative 4. Also, condensation of 3 with p-anisaldehyde gave the corresponding arylidine derivative 5. Treatment of 2 with dimethyl sulfate afforded the ketene N,S-acetal 9 which give 5-amino pyrazole derivative 10 upon treatment with hydrazine hydrate. Compound 10 was used as key intermediate for synthesis of pyrazolo[5,1-c][1,2,4]triazine 13a, b, pyrazolo[5,1-a]pyrimidine 14-17 and pyrolo pyrazole 18 derivatives. Finally, condensation of 1 with DMF-DMA afforded the corresponding acryloamide derivative 19, which afforded the corresponding pyrazole derivative 20 upon heating with hydrazine hydrate. All new synthesized compounds were evaluated as antimicrobial agents; some of them exhibited promising activities.

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