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3122-85-8

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3122-85-8 Usage

General Description

Pyrimidine, 4-amino-2-(ethoxymethyl)- (8CI) is a chemical compound with the molecular formula C8H12N4O, and a molecular weight of 184.21 g/mol. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound. Pyrimidine, 4-amino-2-(ethoxymethyl)- (8CI) is used as a building block in organic synthesis and medicinal chemistry. It has potential applications in the development of pharmaceutical drugs and agrochemicals. The ethoxymethyl group in the compound may impart certain chemical and biological properties, making it a valuable tool in the field of chemical research and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 3122-85-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,2 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3122-85:
(6*3)+(5*1)+(4*2)+(3*2)+(2*8)+(1*5)=58
58 % 10 = 8
So 3122-85-8 is a valid CAS Registry Number.

3122-85-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(methoxymethyl)pyrimidin-4-amine

1.2 Other means of identification

Product number -
Other names QC-5538

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:3122-85-8 SDS

3122-85-8Downstream Products

3122-85-8Relevant articles and documents

Synthesis and biological evaluations of new pyrrolo[2,3-b]pyrimidine as SDI analogs

Guillard, Jerome,Viaud-Massuard, Marie-Claude

, p. 1163 - 1189 (2008/12/20)

The synthesis of new pyrrolo[2,3-d]pyrimidines variously substituted on the N-1 and C-2 atoms are described. Access to these compounds, which have modest activity compared with the first inhibitor SDI, involves, as the key step, the formation of a pyrrolopyrimidine skeleton from the 5-amino-2-(methoxymethyl)pyrimidine.

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