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[4-(1-bromoethyl)phenyl]-2-thienyl ketone is a chemical compound with a molecular formula C14H11BrOS. It is a thienyl ketone derivative that contains a 1-bromoethylphenyl substituent. [4-(1-bromoethyl)phenyl]-2-thienyl ketone is known for its potential applications in various fields, making it a significant target for research and development.

52779-83-6

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52779-83-6 Usage

Uses

Used in Pharmaceutical Synthesis:
[4-(1-bromoethyl)phenyl]-2-thienyl ketone is used as an intermediate in the synthesis of pharmaceuticals for its unique chemical properties. It contributes to the development of new drugs by providing a structural foundation that can be further modified to achieve desired therapeutic effects.
Used in Agrochemical Production:
In the agrochemical industry, [4-(1-bromoethyl)phenyl]-2-thienyl ketone is used as a building block for the creation of various agrochemicals. Its incorporation into these products can enhance their effectiveness in protecting crops and improving agricultural yields.
Used in Materials Science:
[4-(1-bromoethyl)phenyl]-2-thienyl ketone may have potential applications in materials science due to its unique structural properties. It could be utilized in the development of new materials with specific characteristics, such as improved stability or enhanced performance in certain conditions.
Used in Organic Chemistry Research:
As a valuable compound in organic chemistry, [4-(1-bromoethyl)phenyl]-2-thienyl ketone is used in research to explore new reactions and mechanisms. Its study can lead to a better understanding of chemical processes and the discovery of novel synthetic pathways for creating complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 52779-83-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,7 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52779-83:
(7*5)+(6*2)+(5*7)+(4*7)+(3*9)+(2*8)+(1*3)=156
156 % 10 = 6
So 52779-83-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H11BrOS/c1-9(14)10-4-6-11(7-5-10)13(15)12-3-2-8-16-12/h2-9H,1H3

52779-83-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(1-bromoethyl)phenyl]-2-thienyl ketone

1.2 Other means of identification

Product number -
Other names <4-(1-Bromethyl)phenyl>(2-thienyl)methanon

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:52779-83-6 SDS

52779-83-6Upstream product

52779-83-6Relevant academic research and scientific papers

Aroyl-substituted phenylacetic acid derivatives

-

, (2008/06/13)

Compounds of the class of aroyl-substituted phenylacetic acids and corresponding esters, amides and hydroxamic acids, useful as anti-inflammatory agents and certain novel precursors therefor.

Synthesis of α methyl 4 (2 thienylcarbonyl)benzeneacetic acid, suprofen, and derivatives

van Daele,Boey,Sipido,De Bruyn,Janssen

, p. 1495 - 1501 (2007/10/05)

A series of compounds with general structure Het CO Ar CH(CH3)COOH was prepared for pharmacological screening. Different synthetic approaches are described. α Methyl 4 (2 thienylcarbonyl)benzeneacetic acid (compound III-l, suprofen), was found to show a marked antiwrithing activity. Furthermore this compound proved to be a potent inhibitor of prostaglandin biosynthesis.

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