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2-(Benzylthio)-5-bromopyrimidine is an organic heterocyclic compound with the chemical formula C11H9BrN2S. It features a pyrimidine ring with a bromine atom at the 5nd position and a benzylthio group attached to the 2nd position. 2-(Benzylthio)-5-bromopyrimidine has potential pharmaceutical applications due to its structural features and biological activities, making it a valuable building block for medicinal chemistry research and drug discovery.

79686-18-3

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79686-18-3 Usage

Uses

Used in Pharmaceutical Industry:
2-(Benzylthio)-5-bromopyrimidine is used as a chemical intermediate for the development of novel drugs for various therapeutic targets. Its unique structural features and biological activities contribute to its potential as a promising candidate in medicinal chemistry research and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 79686-18-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,8 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 79686-18:
(7*7)+(6*9)+(5*6)+(4*8)+(3*6)+(2*1)+(1*8)=193
193 % 10 = 3
So 79686-18-3 is a valid CAS Registry Number.

79686-18-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzylsulfanyl-5-bromopyrimidine

1.2 Other means of identification

Product number -
Other names 2-(Benzylthio)-5-bromopyrimidine

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:79686-18-3 SDS

79686-18-3Relevant academic research and scientific papers

Pyrimidine-2-sulphides and their S-oxides for use in medicine and methods of use therefor, pharmaceutical compositions containing them, processes for their preparation and per se novel sulphides and S-oxides

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, (2008/06/13)

Compounds of the formula STR1 (wherein X represents a halogen atom; n is 0, 1 or 2; R1 and R2, which may be the same or different, each represents a hydrogen atom or a carboxyl, esterified carboxyl, amido or mono- or di-C1-4 alkylamido group or a C1-4 alkyl group which may if desired carry a carboxyl or esterified carboxyl group; and R3 represents a C1-32 saturated or unsaturated, straight or branched, cyclic or acyclic aliphatic group or an araliphatic or heterocyclic substituted aliphatic group, a heterocyclic group or an aryl group which groups may if desired carry one or more substituents selected from halogen atoms and oxo, nitro, hydroxy, etherified hydroxy, esterified hydroxy, primary, secondary or tertiary amino, acylamino etherified mercapto or S=O or --SO2 derivatives thereof and esterified phosphonic acid groups) and, where an acidic or basic group is present, physiologically compatible salts thereof have been found to be of use in combating abnormal cell proliferation. The compounds are prepared inter alia by oxidation of the corresponding sulfide, displacement of a leaving atom or group from the 2-position of the pyrimidine by reaction with a sulfinic acid or by ring closure of the pyrimidine ring.

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