Cas 1314186-13-4,N-[(4-bromophenyl)(2-methylimidazo[1,2-a]pyridin-3-yl)methyl]-4-phenyl-1,3-thiazol-2-amine

1314186-13-4

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Basic information

Product Name: N-[(4-bromophenyl)(2-methylimidazo[1,2-a]pyridin-3-yl)methyl]-4-phenyl-1,3-thiazol-2-amine
Synonyms: N-[(4-bromophenyl)(2-methylimidazo[1,2-a]pyridin-3-yl)methyl]-4-phenyl-1,3-thiazol-2-amine
CAS NO:1314186-13-4
Molecular Formula:
Molecular Weight: 475.412
EINECS: N/A
Product Categories: N/A
Mol File: 1314186-13-4.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-[(4-bromophenyl)(2-methylimidazo[1,2-a]pyridin-3-yl)methyl]-4-phenyl-1,3-thiazol-2-amine(CAS DataBase Reference)
NIST Chemistry Reference: N-[(4-bromophenyl)(2-methylimidazo[1,2-a]pyridin-3-yl)methyl]-4-phenyl-1,3-thiazol-2-amine(1314186-13-4)
EPA Substance Registry System: N-[(4-bromophenyl)(2-methylimidazo[1,2-a]pyridin-3-yl)methyl]-4-phenyl-1,3-thiazol-2-amine(1314186-13-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1314186-13-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1314186-13-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,1,8 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1314186-13:
(9*1)+(8*3)+(7*1)+(6*4)+(5*1)+(4*8)+(3*6)+(2*1)+(1*3)=124
124 % 10 = 4
So 1314186-13-4 is a valid CAS Registry Number.

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1314186-13-4Relevant articles and documents

A tandem aza-Friedel-Crafts reaction/Hantzsch cyclization: A simple procedure to access polysubstituted 2-amino-1,3-thiazoles

Chaubet, Guihlem,Maillard, Ludovic T.,Martinez, Jean,Masurier, Nicolas

, p. 4897 - 4904 (2011/07/31)

A tandem aza-Friedel-Crafts reaction/Hantzsch cyclization is described to access various polysubstituted 2-amino-1,3-thiazoles from electron-rich (hetero)-aromatic rings, aldehydes, thiourea and α-chloroketones.

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