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2253-05-6

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2253-05-6 Usage

Chemical compound

2-AMINO-4-HYDROXY-6-FLUOROPYRIMIDINE

Molecular weight

127.09 g/mol

Properties

Pyrimidine derivative with an amino group at the 2-position, a hydroxy group at the 4-position, and a fluorine atom at the 6-position

Potential applications

Pharmaceuticals and agrochemicals

Usage

Intermediate for the synthesis of various drugs and pesticides

Importance

Further research and development could lead to the discovery of new and valuable compounds with important biological and industrial activities.

Check Digit Verification of cas no

The CAS Registry Mumber 2253-05-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,5 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2253-05:
(6*2)+(5*2)+(4*5)+(3*3)+(2*0)+(1*5)=56
56 % 10 = 6
So 2253-05-6 is a valid CAS Registry Number.

2253-05-6SDS

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 2-amino-6-fluoro-1H-pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names CTK4E9655

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:2253-05-6 SDS

2253-05-6Downstream Products

2253-05-6Relevant articles and documents

Hydrolytic Stability of Ammo-substituted Difluoropyrimidines

Popova,Studentsov

, p. 435 - 438 (2007/10/03)

Hydrolytic stability of a series of amino-substituted difluoropyrimidines in the pH range 1.4-12.5 at 20°C is studied. The rate constants of aklaline hydrolysis at pH 12.5 are determined, and the effect of substituents in the heterocycle on the rate of alkaline hydrolysis is demonstrated.

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