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388-21-6

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388-21-6 Usage

General Description

The chemical (2-benzoylphenyl)(4-fluorophenyl)methanone is a compound that is composed of a benzoylphenyl group and a fluorophenyl group connected to a methanone moiety. It is a ketone compound with the molecular formula C20H15FO. This chemical has been studied for its potential pharmaceutical applications, such as in the development of new drugs and medications. Its properties and potential uses may make it a valuable compound for further research and development in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 388-21-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 388-21:
(5*3)+(4*8)+(3*8)+(2*2)+(1*1)=76
76 % 10 = 6
So 388-21-6 is a valid CAS Registry Number.

388-21-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(4-fluorobenzoyl)phenyl]-phenylmethanone

1.2 Other means of identification

Product number -
Other names -

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:388-21-6 SDS

388-21-6Downstream Products

388-21-6Relevant 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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