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7577-92-6

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7577-92-6 Usage

General Description

5-Methylaminouracil is a chemical compound that belongs to the class of nucleobases. It is a derivative of uracil, containing a methylamino group at the 5th position of the pyrimidine ring. This chemical is not naturally occurring in the body but can be synthesized in the laboratory for research and pharmaceutical purposes. It has been studied for its potential application in the fields of medicine and biochemistry, particularly in the development of antiviral and antineoplastic drugs. 5-Methylaminouracil has also been investigated for its role in nucleic acid structure and function, as well as its potential as a molecular tool in genetic engineering and molecular biology research.

Check Digit Verification of cas no

The CAS Registry Mumber 7577-92-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,7 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7577-92:
(6*7)+(5*5)+(4*7)+(3*7)+(2*9)+(1*2)=136
136 % 10 = 6
So 7577-92-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H7N3O2/c1-6-3-2-7-5(10)8-4(3)9/h2,6H,1H3,(H2,7,8,9,10)

7577-92-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(methylamino)-1H-pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-Methylamino-uracil

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:7577-92-6 SDS

7577-92-6Relevant articles and documents

Photochemical reactions of 5-fluoropyrimidine bases with selected alkylamines

Kanciurzewska, Anna,Raczkowski, Mateusz,Ciszewski, Krzysztof,Celewicz, Lech

, p. 761 - 763 (2007/10/03)

Novel photochemical reactions between 5-fluoropyrimidine bases and primary alkylamines are described. Photoreaction of 5-fluorouracil with alkylamines in aqueous solution (pH>8) leads to 5-alkylaminouracils as the main photoproducts. Similarly, photoreact

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