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5778-00-7

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5778-00-7 Usage

General Description

(2-benzoylphenyl)(4-chlorophenyl)methanone is a chemical compound with the molecular formula C22H15ClO and a molecular weight of 330.80 g/mol. It is a ketone derivative with two aromatic benzene rings, one of which is substituted with a benzoyl group and the other with a chlorophenyl group. (2-benzoylphenyl)(4-chlorophenyl)methanone is commonly used in organic synthesis and pharmaceutical research due to its potential applications in the development of drugs and other biologically active compounds. It may also have properties that make it useful in the synthesis of materials with specific properties in various fields such as materials science and nanotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 5778-00-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,7 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5778-00:
(6*5)+(5*7)+(4*7)+(3*8)+(2*0)+(1*0)=117
117 % 10 = 7
So 5778-00-7 is a valid CAS Registry Number.

5778-00-7SDS

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-(4-chlorobenzoyl)phenyl]-phenylmethanone

1.2 Other means of identification

Product number -
Other names 2-benzoyl-4-bromophenol

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:5778-00-7 SDS

5778-00-7Downstream Products

5778-00-7Relevant articles and documents

Copper-catalyzed benzylic C-H oxygenation under an oxygen atmosphere via N-H imines as an intramolecular directing group

Zhang, Line,Ang, Gim Yean,Chiba, Shunsuke

, p. 1622 - 1625 (2011/05/05)

Copper-catalyzed benzylic C-H oxygenation under an oxygen atmosphere was developed starting from carbonitriles and Grignard reagents via N-H imine intermediates. The present process is characterized by the following two-step sequence in a one-pot manner: (1) addition of Grignard reagents to carbonitriles to form N-H imines and (2) benzylic C-H oxygenation (C=O bond formation) triggered by 1,5-hydrogen atom transfer with transient iminyl copper species.

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