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56004-62-7

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56004-62-7 Usage

Description

(3-methylthiophen-2-yl)(phenyl)methanone is a chemical compound with the molecular formula C15H12OS. It is a ketone that consists of a phenyl group attached to a thiophene ring with a methyl group at the 3-position. (3-methylthiophen-2-yl)(phenyl)methanone is known for its potential applications in various fields due to its unique structure and properties.

Uses

Used in Organic Synthesis:
(3-methylthiophen-2-yl)(phenyl)methanone is used as a building block in organic synthesis for the creation of complex organic molecules. Its unique structure allows for versatile reactions and the formation of a wide range of compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3-methylthiophen-2-yl)(phenyl)methanone serves as a valuable starting material for the synthesis of biologically active molecules. Its potential to be modified and combined with other compounds makes it a promising candidate for drug development.
Used as an Anti-inflammatory Agent:
(3-methylthiophen-2-yl)(phenyl)methanone has been studied for its potential pharmacological properties, including its use as an anti-inflammatory agent. Its ability to reduce inflammation can be beneficial in the treatment of various conditions.
Used as an Analgesic Agent:
Additionally, (3-methylthiophen-2-yl)(phenyl)methanone has shown potential as an analgesic agent, which can help alleviate pain. This property makes it a candidate for the development of new pain management therapies.
Overall, (3-methylthiophen-2-yl)(phenyl)methanone is an important and versatile chemical compound with potential applications in various fields, including organic synthesis, pharmaceutical research, and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 56004-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,0 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56004-62:
(7*5)+(6*6)+(5*0)+(4*0)+(3*4)+(2*6)+(1*2)=97
97 % 10 = 7
So 56004-62-7 is a valid CAS Registry Number.

56004-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methylthiophen-2-yl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names 2-Benzoyl-3-methylthiophrn

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:56004-62-7 SDS

56004-62-7Downstream Products

56004-62-7Relevant articles and documents

Coupling of aromatic aldehydes with aryl halides in the presence of nickel catalysts with diazabutadiene ligands

Asachenko,Valaeva,Kudakina,Uborsky,Izmer,Kononovich,Voskoboynikov

, p. 456 - 463 (2017/03/08)

Nickel catalysts with diazabutadiene ligands promote cross-coupling of benzaldehydes with aryl halides in the presence of zinc as reducing agent, which leads to the corresponding benzhydrols and benzophenones. The benzophenone percentage considerably increases when lithium chloride additive is used.

A highly active ytterbium(III) methide complex for truly catalytic Friedel-Crafts acylation reactions

Barrett, Anthony G. M.,Bouloc, Nathalie,Braddock, D. Christopher,Chadwick, David,Henderson, David A.

, p. 1653 - 1656 (2007/10/03)

The Friedel-Crafts acylation of anisole with acetic anhydride using ytterbium(III) tri[tris(nonafluorobutanesulfonyl)methide] was studied with respect to catalyst loading. A strong inhibitory effect due to the product became apparent from doping experiments and from examination of the kinetic data. This understanding allowed catalyst loadings to be reduced to as little as 0.1 mol% for effective acylation under a suitable temperature and pressure regime.

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