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99429-06-8

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99429-06-8 Usage

Chemical structure

heterocyclic aromatic compound with a pyrimidine ring

Substituents

fluorine atoms at the 2 and 5 positions, chlorine atom at the 4 position

Uses

building block in pharmaceutical synthesis, intermediate in agrochemical production, used in the synthesis of biologically active molecules

Versatility

valuable chemical with multiple applications in drug discovery and chemical synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 99429-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,4,2 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 99429-06:
(7*9)+(6*9)+(5*4)+(4*2)+(3*9)+(2*0)+(1*6)=178
178 % 10 = 8
So 99429-06-8 is a valid CAS Registry Number.

99429-06-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Pyrimidine, 4-chloro-2,5-difluoro-

1.2 Other means of identification

Product number -
Other names 4-Chloro-2,5-difluoropyrimidine

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:99429-06-8 SDS

99429-06-8Relevant articles and documents

A NEW ROUTE TO THE SYNTHESIS OF 5-FLUOROURACIL

Baasner, B.,Klauke, E.

, p. 417 - 430 (2007/10/02)

Starting from tetrafluoropyrimidine (1), selective fluorine/chlorine exchange reactions and selective hydrogenolysis of the chlorine substituents are described.Combination of these methods, together with a subsequent hydrolysis reaction, provides a new route to the synthesis of 5-fluorouracil via 4,6-dichloro-2,5-difluoropyrimidine and 4-chloro-2,5-difluoropyrimidine.

Process for the preparation of 5-fluorocytosine

-

, (2008/06/13)

5-fluorocytosine is prepared by reacting 2,5-difluoro-4-chloro-pyrimidine with a proton acid in the presence of water to yield 2-hydroxy-4-chloro-5-fluoropyrimidine and reacting the 2-hydroxy-4-chloro-5-fluoropyrimidine with ammonia to yield 5-fluoro-cytosine.

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