Cas 159448-63-2,2-butyl-4-chloro-5-(hydroxymethyl)-1-<<2-<2-(methoxycarbonyl)phenyl>thien-5-yl>methyl>-1H-imidazole

159448-63-2

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Basic information

Product Name: 2-butyl-4-chloro-5-(hydroxymethyl)-1-<<2-<2-(methoxycarbonyl)phenyl>thien-5-yl>methyl>-1H-imidazole
Synonyms: 2-butyl-4-chloro-5-(hydroxymethyl)-1-<<2-<2-(methoxycarbonyl)phenyl>thien-5-yl>methyl>-1H-imidazole
CAS NO:159448-63-2
Molecular Formula:
Molecular Weight: 418.944
EINECS: N/A
Product Categories: N/A

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: 2-butyl-4-chloro-5-(hydroxymethyl)-1-<<2-<2-(methoxycarbonyl)phenyl>thien-5-yl>methyl>-1H-imidazole(CAS DataBase Reference)
NIST Chemistry Reference: 2-butyl-4-chloro-5-(hydroxymethyl)-1-<<2-<2-(methoxycarbonyl)phenyl>thien-5-yl>methyl>-1H-imidazole(159448-63-2)
EPA Substance Registry System: 2-butyl-4-chloro-5-(hydroxymethyl)-1-<<2-<2-(methoxycarbonyl)phenyl>thien-5-yl>methyl>-1H-imidazole(159448-63-2)

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: 159448-63-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 159448-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,4,4 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 159448-63:
(8*1)+(7*5)+(6*9)+(5*4)+(4*4)+(3*8)+(2*6)+(1*3)=172
172 % 10 = 2
So 159448-63-2 is a valid CAS Registry Number.

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159448-63-2Relevant academic research and scientific papers

Nonpeptide Angiotensin II Receptor Antagonists. Synthesis, in Vitro Activity, and Molecular Modeling Studies of N-imidazoles

Salimbeni, Aldo,Canevotti, Renato,Paleari, Fabio,Bonaccorsi, Fabrizio,Renzetti, Anna R.,et al.

, p. 3928 - 3938 (2007/10/02)

With the aim of explaining the influence of the structural changes on the biphenylic moiety on the activity, a series of N-imidazoles (I), constructed on the model of DuPont compounds by replacing either the central or terminal pheny

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