Cas 201280-81-1,4-(4-bromophenyl)-6-{[2-(4-bromophenyl)-2-oxoethyl]sulfanyl}-5-cyano-2-methyl-N-phenylnicotinamide

201280-81-1

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Basic information

Product Name: 4-(4-bromophenyl)-6-{[2-(4-bromophenyl)-2-oxoethyl]sulfanyl}-5-cyano-2-methyl-N-phenylnicotinamide
Synonyms: 4-(4-bromophenyl)-6-{[2-(4-bromophenyl)-2-oxoethyl]sulfanyl}-5-cyano-2-methyl-N-phenylnicotinamide
CAS NO:201280-81-1
Molecular Formula: C28H19Br2N3O2S
Molecular Weight: 621.34236
EINECS: N/A
Product Categories: N/A
Mol File: 201280-81-1.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-(4-bromophenyl)-6-{[2-(4-bromophenyl)-2-oxoethyl]sulfanyl}-5-cyano-2-methyl-N-phenylnicotinamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-(4-bromophenyl)-6-{[2-(4-bromophenyl)-2-oxoethyl]sulfanyl}-5-cyano-2-methyl-N-phenylnicotinamide(201280-81-1)
EPA Substance Registry System: 4-(4-bromophenyl)-6-{[2-(4-bromophenyl)-2-oxoethyl]sulfanyl}-5-cyano-2-methyl-N-phenylnicotinamide(201280-81-1)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 201280-81-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 201280-81-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,2,8 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 201280-81:
(8*2)+(7*0)+(6*1)+(5*2)+(4*8)+(3*0)+(2*8)+(1*1)=81
81 % 10 = 1
So 201280-81-1 is a valid CAS Registry Number.

201280-81-1Upstream product

201280-81-1Downstream Products

201280-81-1Relevant academic research and scientific papers

Acetoacetanilides in synthesis of 4-aryl-5-arylcarbamoyl-6-methyl-s-cyanopyridine-2(1H)-thiones

Dyachenko,Krivokolysko,Litvinov

, p. 481 - 488 (2007/10/03)

The reaction of acetoacetanilides with arylmethylenecyanothioacetamides leads to 4-aryl-5-arylcarbamoyl-6-methyl-3-cyanopyridine-2(1H)-thiones, based on which we have obtained substituted 2-alkylthiopyridines and thieno[2,3-b]pyridines. 1997 Plenum Publishing Corporation.

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