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22874-42-6

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22874-42-6 Usage

Chemical Class

Pyrimidine

Derivative

Thioxopyrimidin

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Biological Activities

Antimicrobial and antifungal properties

Research Applications

Study of various diseases and disorders, development of new drugs

Form

Monosodium salt

Benefits of Monosodium Salt Form

Easier handling and dissolution in aqueous solutions, versatile and valuable chemical in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 22874-42-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,7 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22874-42:
(7*2)+(6*2)+(5*8)+(4*7)+(3*4)+(2*4)+(1*2)=116
116 % 10 = 6
So 22874-42-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2OS.Na/c1-3-2-4(8)7-5(9)6-3;/h2H,1H3,(H2,6,7,8,9);/q;+1/p-1

22874-42-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,6-methyl-2-sulfanylidene-1H-pyrimidin-3-id-4-one

1.2 Other means of identification

Product number -
Other names sodium salt of 4-methyl-2-thiouracil

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:22874-42-6 SDS

22874-42-6Relevant articles and documents

Special features of the nucleophilic substitution of halogen in alkyl and benzyl halides with anions generated from 4-hydroxy-2-mercapto-6- methylpyrimidine

Rakhimov,Titova,Fedunov,Babkin, Vladimir Aleksandrovich

experimental part, p. 700 - 708 (2009/04/06)

The nucleophilic substitution of halogen (chlorine, bromine, and iodine) in alkyl and benzyl halides has been effected in aqueous dioxane media with S-and O-anions generated from 4-hydroxy-2-mercapto-6-methylpyrimidine. Under these conditions replacement

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