Cas 142385-50-0,2-Butyl-4-(4-chloro-phenyl)-6-methyl-1,6-dihydro-pyrimidine-5-carboxylic acid ethyl ester

142385-50-0

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Basic information

Product Name: 2-Butyl-4-(4-chloro-phenyl)-6-methyl-1,6-dihydro-pyrimidine-5-carboxylic acid ethyl ester
Synonyms:
CAS NO:142385-50-0
Molecular Formula:
Molecular Weight: 334.846
EINECS: N/A
Product Categories: N/A
Mol File: 142385-50-0.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: 2-Butyl-4-(4-chloro-phenyl)-6-methyl-1,6-dihydro-pyrimidine-5-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Butyl-4-(4-chloro-phenyl)-6-methyl-1,6-dihydro-pyrimidine-5-carboxylic acid ethyl ester(142385-50-0)
EPA Substance Registry System: 2-Butyl-4-(4-chloro-phenyl)-6-methyl-1,6-dihydro-pyrimidine-5-carboxylic acid ethyl ester(142385-50-0)

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: 142385-50-0(Hazardous Substances Data)

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142385-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142385-50-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,3,8 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 142385-50:
(8*1)+(7*4)+(6*2)+(5*3)+(4*8)+(3*5)+(2*5)+(1*0)=120
120 % 10 = 0
So 142385-50-0 is a valid CAS Registry Number.

142385-50-0Upstream product

18257-46-0 pentanamidine hydrochloride

142385-50-0Downstream Products

142385-51-1 1-(2'-tert-Butoxycarbonyl-biphenyl-4-ylmethyl)-2-butyl-4-(4-chloro-phenyl)-6-methyl-1,6-dihydro-pyrimidine-5-carboxylic acid ethyl ester

142385-50-0Relevant articles and documents

Dihydropyrimidine Angiotensin II Receptor Antagonists

Atwal, Karnail S.,Ahmed, Syed Z.,Bird, J. Eileen,Delaney, Carol L.,Dickinson, Kenneth E. J.,et al.

, p. 4751 - 4763 (2007/10/02)

The discovery of the nonpeptidic angiotensin II (AII) receptor antagonist losartan (1), previously called DuP 753, has stimulated considerable interest in the synthesis of novel analogs of this compound.Our efforts in this urea have resulted in the discov

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