Cas 148549-79-5,1H-Imidazole-5-carboxylic acid, 2-butyl-4-chloro-1-[[4-[[2-[2-(methoxycarbonyl)-1H-pyrrol-1-yl]-1-oxo-3-( 2-thienyl)propyl]amino]phenyl]methyl]-, methyl ester, (S)-

148549-79-5

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Basic information

Product Name: 1H-Imidazole-5-carboxylic acid, 2-butyl-4-chloro-1-[[4-[[2-[2-(methoxycarbonyl)-1H-pyrrol-1-yl]-1-oxo-3-( 2-thienyl)propyl]amino]phenyl]methyl]-, methyl ester, (S)-
Synonyms:
CAS NO:148549-79-5
Molecular Formula: C29H31ClN4O5S
Molecular Weight: 583.108
EINECS: N/A
Product Categories: N/A
Mol File: 148549-79-5.mol

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: 1H-Imidazole-5-carboxylic acid, 2-butyl-4-chloro-1-[[4-[[2-[2-(methoxycarbonyl)-1H-pyrrol-1-yl]-1-oxo-3-( 2-thienyl)propyl]amino]phenyl]methyl]-, methyl ester, (S)-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Imidazole-5-carboxylic acid, 2-butyl-4-chloro-1-[[4-[[2-[2-(methoxycarbonyl)-1H-pyrrol-1-yl]-1-oxo-3-( 2-thienyl)propyl]amino]phenyl]methyl]-, methyl ester, (S)-(148549-79-5)
EPA Substance Registry System: 1H-Imidazole-5-carboxylic acid, 2-butyl-4-chloro-1-[[4-[[2-[2-(methoxycarbonyl)-1H-pyrrol-1-yl]-1-oxo-3-( 2-thienyl)propyl]amino]phenyl]methyl]-, methyl ester, (S)-(148549-79-5)

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: 148549-79-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 148549-79-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,5,4 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 148549-79:
(8*1)+(7*4)+(6*8)+(5*5)+(4*4)+(3*9)+(2*7)+(1*9)=175
175 % 10 = 5
So 148549-79-5 is a valid CAS Registry Number.

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148549-79-5Relevant academic research and scientific papers

Nonpeptide angiotensin II receptor antagonists. 1. Synthesis and in vitro structure-activity relationships of 4[[[(1H-pyrrol-1- ylacetyl)amino]phenyl]methyl]imidazole derivatives as angiotensin II receptor antagonists

Sircar,Winters,Quin III,Lu,Major,Panek

, p. 1735 - 1745 (2007/10/02)

A novel series of non-biphenylyltetrazole angiotensin II receptor antagonists which contain a 1H-pyrrol-1-ylacetyl residue in place of the benzoyl residue in EXP 6803 have been developed. The receptor binding activity of several members of this new series

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