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5-{3,5-dimethoxy-4-[(1E)-prop-1-en-1-yl]benzyl}pyrimidine-2,4-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69194-91-8

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69194-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69194-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,1,9 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69194-91:
(7*6)+(6*9)+(5*1)+(4*9)+(3*4)+(2*9)+(1*1)=168
168 % 10 = 8
So 69194-91-8 is a valid CAS Registry Number.

69194-91-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[[3,5-dimethoxy-4-[(E)-prop-1-enyl]phenyl]methyl]pyrimidine-2,4-diamine

1.2 Other means of identification

Product number -
Other names 5-((3,5-Dimethoxy-4-(1-methylethenyl)phenyl)methyl)-2,4-pyrimidinediamine

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:69194-91-8 SDS

69194-91-8Relevant academic research and scientific papers

Benzylpyrimidine derivatives

-

, (2008/06/13)

Benzylpyrimidines of the formula STR1 wherein R1 and R2, independently, are C1-6 -alkyl, R3 is C1-3 -alkyl and R4 is methylene or C2-4 -alkylidene and physiologically compatible

Synthesis and antimicrobial activity of C(4')-substituted analogs of trimethoprim

Kompis,Then,Boehni,et al.

, p. 17 - 22 (2007/10/02)

A series of 2,4-diamino-5-(3,5-dimethoxybenzyl)-pyrimidines substitute at C(4') of the benzene ring with a functionalized carbon atom was synthesized. The target substances were tested for inhibition of dihydrofolate reductases from E. coli and rat liver,

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