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18793-94-7

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18793-94-7 Usage

General Description

The chemical (2-benzylphenyl)(4-chlorophenyl)methanone, also known as 4’-chloro-benzylphenyl methanone, is a benzophenone derivative compound. It is a ketone that consists of a benzylphenyl group and a 4-chlorophenyl group attached to the carbonyl carbon atom. (2-benzylphenyl)(4-chlorophenyl)methanone is used in the synthesis of various pharmaceuticals and organic compounds. It possesses anti-inflammatory and analgesic properties, making it a potential candidate for drug development. Additionally, it is also utilized in the production of ultraviolet (UV) stabilizers and photoinitiators for plastics and polymers. Its unique chemical structure and properties make it a valuable compound in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 18793-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,9 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18793-94:
(7*1)+(6*8)+(5*7)+(4*9)+(3*3)+(2*9)+(1*4)=157
157 % 10 = 7
So 18793-94-7 is a valid CAS Registry Number.

18793-94-7SDS

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 2-benzyl-4'-chloro-benzophenone

1.2 Other means of identification

Product number -
Other names 2-Benzyl-4'-chlor-benzophenon

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:18793-94-7 SDS

18793-94-7Relevant articles and documents

Synthesis of 2-Benzylphenyl Ketones by Aryne Insertion into Unactivated C-C Bonds

Rao, Bin,Tang, Jinghua,Zeng, Xiaoming

supporting information, p. 1678 - 1681 (2016/04/26)

A transition-metal-free procedure to access to functionalized 2-benzylphenyl ketones is described by direct insertion of arynes into benzylic C-C bonds. This reaction was promoted by cesium fluoride at room temperature, allowing the products to form in high selectivity and achieve good functional group tolerance.

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