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5-Pyrimidinecarboxylic acid, 4-[4-(methoxycarbonyl)phenyl]-6-methyl-2-phenyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103293-93-2

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103293-93-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103293-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,2,9 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 103293-93:
(8*1)+(7*0)+(6*3)+(5*2)+(4*9)+(3*3)+(2*9)+(1*3)=102
102 % 10 = 2
So 103293-93-2 is a valid CAS Registry Number.

103293-93-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-(4-methoxycarbonylphenyl)-6-methyl-2-phenyl-5-pyrimidinecarboxylate

1.2 Other means of identification

Product number -
Other names 4-(4-Methoxycarbonyl-phenyl)-6-methyl-2-phenyl-pyrimidine-5-carboxylic acid ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:103293-93-2 SDS

103293-93-2Downstream Products

103293-93-2Relevant academic research and scientific papers

Studies on cerebral protective agents. I. Novel 4-arylpyrimidine derivatives with anti-anoxic and anti-lipid peroxidation activities

Kuno,Sugiyama,Katsuta,Kamitani,Takasugi

, p. 1452 - 1461 (2007/10/02)

Novel 4-arylpyrimidine derivatives were synthesized by the oxidation of 4-aryl-1,4-dihydropyrimidines, and their effects on anti-anoxic (AA) activity in mice and anti-lipid peroxidation (ALP) activity in rat brain mitochondria were investigated. Among these compounds, ethyl 6-methyl-2-phenyl-4-(4-pyridyl)-5-pyrimidinecarboxylate (4b) has AA activity (10mg/kg, i.p.) and ethyl 6-methyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxylate (4f) has ALP activity (73% inhibition at 10-5 g/ml). The latter compound (100mg/kg, i.p.) was also effective on arachidonate-induced cerebral edema in rats with comparable potency to that of vitamin E.

Pyrimidine derivatives, processes for preparation thereof and composition containing the same

-

, (2008/06/13)

The invention relates to pyrimidine derivatives and their pharmaceutically acceptable salts which are useful in the treatment of cerebrovascular diseases, to processes for preparation thereof and to the composition containing the same, said pyrimidine der

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