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31458-47-6

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31458-47-6 Usage

Structure

A pyrimidinone ring with an amino group attached to the fourth carbon and a methoxy group attached to the fifth carbon.

Type

A chemical compound and a derivative of pyrimidinone.

Usage

Primarily used in organic synthesis and medicinal chemistry as a building block for the production of various pharmaceuticals and agricultural chemicals.

Biological activity

Exhibits biological activity and has been studied for its potential medicinal applications, particularly in the treatment of neurological and inflammatory conditions.

Versatility

Has applications in both research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 31458-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,4,5 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 31458-47:
(7*3)+(6*1)+(5*4)+(4*5)+(3*8)+(2*4)+(1*7)=106
106 % 10 = 6
So 31458-47-6 is a valid CAS Registry Number.

31458-47-6SDS

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 2(1H)-Pyrimidinone, 4-amino-5-methoxy- (9CI)

1.2 Other means of identification

Product number -
Other names 5-Hydroxymethyl-cytosin

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:31458-47-6 SDS

31458-47-6Downstream Products

31458-47-6Relevant articles and documents

Photochemical reactions of 5-fluoropyrimidine bases with alcohols

Urjasz, Wojciech,Maciejewski, Andrzej,Celewicz, Lech

, p. 3243 - 3246 (1999)

Photochemical reactions of 5-fluorocytosine with primary alcohols led to 5-alkoxycytosines and 6-alkoxycytosines as the main photoproducts. These products are formed via reactive intermediates 6-alkoxy-5-fluoro-5,6- dihydrocytosines, whereas photochemical reactions of 5-fluorouracil with alcohols led to stable 6-alkoxy-5-fluoro-5,6-dihydrouracils.

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