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(3-Bromophenyl)(2-thienyl)Methanone, also known as 2-(3-bromophenyl)thiophen-3-ylmethanone, is a chemical compound with the molecular formula C14H9BrOS. It is a ketone compound that contains a bromophenyl group and a thienyl group. This chemical is commonly used as an intermediate in organic synthesis and pharmaceutical research. It has also been studied for its potential applications in the development of new drugs and other biologically active compounds. As a ketone, (3-Bromophenyl)(2-thienyl)Methanone possesses carbonyl functionality, making it a versatile building block for the creation of diverse organic molecules with various properties and applications.

31161-47-4

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31161-47-4 Usage

Uses

Used in Organic Synthesis:
(3-Bromophenyl)(2-thienyl)Methanone is used as an intermediate in organic synthesis for the creation of diverse organic molecules with various properties and applications.
Used in Pharmaceutical Research:
(3-Bromophenyl)(2-thienyl)Methanone is used as a building block in pharmaceutical research for the development of new drugs and other biologically active compounds.
Used in Drug Development:
(3-Bromophenyl)(2-thienyl)Methanone is used in the development of new drugs and other biologically active compounds due to its potential applications in this field.

Check Digit Verification of cas no

The CAS Registry Mumber 31161-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,6 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 31161-47:
(7*3)+(6*1)+(5*1)+(4*6)+(3*1)+(2*4)+(1*7)=74
74 % 10 = 4
So 31161-47-4 is a valid CAS Registry Number.

31161-47-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name m-bromophenyl-2-thienyl ketone

1.2 Other means of identification

Product number -
Other names (3-Bromophenyl)(thiophen-2-yl)methanone

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:31161-47-4 SDS

31161-47-4Downstream Products

31161-47-4Relevant academic research and scientific papers

Catalytic asymmetric alkylation of aryl heteroaryl ketones

Ortiz, Pablo,Del Hoyo, Ana M.,Harutyunyan, Syuzanna R.

supporting information, p. 72 - 76 (2015/02/19)

Tertiary diarylmethanols are highly bioactive structural motifs. A new strategy to access chiral tertiary diarylmethanols through copper-catalyzed direct alkylation of (di)(hetero)aryl ketones by using Grignard reagents was developed. The low reactivity a

Infrared and Nuclear Magnetic Resonance Properties of Benzoyl Derivatives of Five-membered Monoheterocycles and Determination of Aromaticity Indices

Jeon, Kyu Ok,Jun, Jung Ho,Yu, Ji Sook,Lee, Chang Kiu

, p. 763 - 771 (2007/10/03)

Benzophenones, 2-benzoylthiophenes, 2-benzoylpyrroles, and 2-benzoylfurans, which have substituents at m- and p-positions of the benzoyl ring were prepared and their ir and nmr spectra were obtained in 0.1 M chloroform-d solution. The chemical shift values of each series were plotted against the Hammett substituent parameters to give good correlation, with the exception of the ortho-Hs and -Cs. The slopes as well as the differences in chemical shift gave sets of meaningful values for the indices of aromaticy.

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