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62237-50-7

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62237-50-7 Usage

Structure

Consists of a pyridine ring with a substituted ethyl group and a 4-bromophenylthio substituent.

Application

Used in organic synthesis and pharmaceutical research.

Biological Activities

Potential biological activities and therapeutic applications.

Ligand Activity

Exhibits ligand activity for various biological targets.

Drug Development

Studied for potential use in developing new drugs and therapeutics.

Intermediate Use

Employed as an intermediate in the preparation of various pharmaceutical compounds.

Building Block

Serves as a building block in the production of organic chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 62237-50-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,3 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62237-50:
(7*6)+(6*2)+(5*2)+(4*3)+(3*7)+(2*5)+(1*0)=107
107 % 10 = 7
So 62237-50-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H12BrNS/c14-12-1-3-13(4-2-12)16-10-7-11-5-8-15-9-6-11/h1-6,8-9H,7,10H2

62237-50-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(4-bromophenyl)sulfanylethyl]pyridine

1.2 Other means of identification

Product number -
Other names 2-(4-pyridinyl)ethyl-4'-bromophenyl sulfide

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:62237-50-7 SDS

62237-50-7Relevant articles and documents

Amberlyst-15: An efficient heterogeneous reusable catalyst for selective anti-Markovnikov addition of thiols to alkenes/alkynes and for thiolysis of epoxides

Lanke, Satish R.,Bhanage, Bhalchandra M.

, p. 29 - 33 (2013/08/23)

The anti-Markovnikov addition of thiols to alkenes/alkynes and thiolysis of epoxides is described using Amberlyst-15 as a selective, commercially available, inexpensive and reusable catalyst. The products like diorganyl sulphides, β-hydroxy sulphides and phenyl(styryl)sulfanes were obtained in good to excellent yields in short reaction time and with high regio-selectivity. The catalyst was reused up to five consecutive recycles without any loss in its catalytic activity. The developed methodology is a metal free protocol for C-S bond formation reaction with high atom economy.

Soluble ferrocene conjugates for incorporation into self-assembled monolayers

Yu,Chong, Yoochul,Kayyem, Jon Faiz,Gozin, Michael

, p. 2070 - 2079 (2007/10/03)

A series of phenylethynyl oligomers (I-V) possessing a ferrocene and thiol at each termini have been synthesized. These oligomers have been designed to overcome the inherent insolubility of this class of complexes by substitution at the phenyl groups with methyl and propoxy substituents. Several new reactions for preparing arenethiol-protected compounds are described. Interestingly, the generation of an arenethiol anion during base- or fluoride-catalyzed deprotection has been characterized.

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