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118150-25-7

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118150-25-7 Usage

Molecular structure

A chemical compound consisting of a thiophene ring with a bromobenzyl group attached to it at the 2-position.

Usage

Commonly used in organic synthesis and pharmaceutical research due to its potential pharmacological properties.

Reactivity

The bromobenzyl group increases the compound's reactivity.

Modifications

The bromobenzyl group can be used as a handle for further modifications.

Drug development

Has potential use in the development of new drugs.

Building block

Used as a building block in the synthesis of various organic compounds.

Materials science

Utilized in the production of electronic and optoelectronic devices.

Check Digit Verification of cas no

The CAS Registry Mumber 118150-25-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,1,5 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 118150-25:
(8*1)+(7*1)+(6*8)+(5*1)+(4*5)+(3*0)+(2*2)+(1*5)=97
97 % 10 = 7
So 118150-25-7 is a valid CAS Registry Number.

118150-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-bromophenyl)methyl]thiophene

1.2 Other means of identification

Product number -
Other names -

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:118150-25-7 SDS

118150-25-7Downstream Products

118150-25-7Relevant articles and documents

Selective double Suzuki cross-coupling reactions. Synthesis of unsymmetrical diaryl (or heteroaryl) methanes

Langle, Sandrine,Abarbri, Mohamed,Duchêne, Alain

, p. 9255 - 9258 (2003)

Using a double Suzuki cross-coupling reaction ortho- or para-bromobenzyl bromides are easily transformed into unsymmetrical diaryl (or heteroaryl) methanes.

Rapid Mo(CO)6 catalysed one-pot deoxygenation of heterocyclic halo-benzyl alcohols with Lawesson's reagent

Wu, Xiongyu,Mahalingam,Alterman, Mathias

, p. 1501 - 1504 (2007/10/03)

A fast and efficient microwave promoted one-pot method for deoxygenation of heterocyclic halo-benzyl alcohols has been developed. The method does not cause dehalogenation of the substrates and provides the deoxygenated products in high yield after only 30 min.

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