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132932-62-8

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132932-62-8 Usage

General Description

2-(4-Acetoxyphenyl)benzothiophene is a chemical compound that contains a benzothiophene core with a 4-acetoxyphenyl group attached at the 2-position. It is a synthetic organic compound that is commonly used in the research and development of pharmaceuticals and other chemical applications. It has potential pharmacological properties and has been studied for its potential use in the treatment of various diseases and conditions. It is important to handle this compound with caution, as it may have potential health and safety hazards associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 132932-62-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,9,3 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 132932-62:
(8*1)+(7*3)+(6*2)+(5*9)+(4*3)+(3*2)+(2*6)+(1*2)=118
118 % 10 = 8
So 132932-62-8 is a valid CAS Registry Number.

132932-62-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(1-benzothiophen-2-yl)phenyl] acetate

1.2 Other means of identification

Product number -
Other names 2-(4-acetylphenyl)benzothiophene

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:132932-62-8 SDS

132932-62-8Downstream Products

132932-62-8Relevant articles and documents

Infrared Irradiation-Assisted Solvent-Free Pd-Catalyzed (Hetero)aryl-aryl Coupling via C?H Bond Activation

Albano, Gianluigi,Decandia, Gianfranco,Capozzi, Maria Annunziata M.,Zappimbulso, Nicola,Punzi, Angela,Farinola, Gianluca M.

, p. 3391 - 3401 (2021/07/28)

The increasing attention towards environmentally friendly synthetic protocols has boosted studies directed to the development of green and sustainable methods for direct C?H bond arylation of (hetero)arenes. In this context, here the infrared (IR) irradia

A tridentate CNO-donor palladium(II) complex as efficient catalyst for direct C―H arylation: Application in preparation of imidazole-based push–pull chromophores

Li, Hui-Hong,Maitra, Ratnava,Kuo, Ya-Ting,Chen, Jie-Hong,Hu, Ching-Han,Lee, Hon Man

, (2017/09/06)

A series of imidazolium chlorides for the formation of tridentate CNO-donor palladium(II) complexes featuring N-heterocyclic carbene moieties have been developed from cheap and readily available starting materials with high yields. Their palladium complex

Method for synthesizing benzothiophene derivative by catalysis of dihalogenated aromatics by copper

-

Paragraph 0026; 0052, (2018/08/28)

The invention discloses a method for synthesizing a benzothiophene derivative by catalysis of dihalogenated aromatics by copper. According to the invention, a catalyst cuprous iodide with a catalysisamount, a ligand 8-hydroxyquinoline, an auxiliary catalyst cesium carbonate and 1-bromine-2-iodobenzene or its derivative, sulfur powder, and phenylacetylene or its derivative are added in a flask andsubjected to a reaction in pure water at certain temperature, after a certain time, vacuum concentration is carried out, and a product is purified through column chromatography. The method has the advantages of novel raw material and simple operation, and can be used for efficiently preparing the benzothiophene derivative. Compared with the prior art, the method has the advantages of mild reaction condition, simple operation, high yield, safety, low cost, and environmental protection.

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