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103060-18-0

103060-18-0

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103060-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103060-18-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,0,6 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 103060-18:
(8*1)+(7*0)+(6*3)+(5*0)+(4*6)+(3*0)+(2*1)+(1*8)=60
60 % 10 = 0
So 103060-18-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H11ClO3/c1-10(17)19-14-8-4-12(5-9-14)15(18)11-2-6-13(16)7-3-11/h2-9H,1H3

103060-18-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(4-chlorobenzoyl)phenyl] acetate

1.2 Other means of identification

Product number -
Other names 4-ACETOXY-4'-CHLOROBENZOPHENONE

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:103060-18-0 SDS

103060-18-0Downstream Products

103060-18-0Relevant articles and documents

Synthesis of unsymmetrical ketones by applying visible-light benzophenone/nickel dual catalysis for direct benzylic acylation

Krach, Patricia E.,Dewanji, Abhishek,Yuan, Tingting,Rueping, Magnus

supporting information, p. 6082 - 6085 (2020/06/18)

Herein, we report a dual catalytic system for the direct benzylic C-H acylation reaction furnishing a variety of unsymmetrical ketones. A benzophenone-derived photosensitizer combined with a nickel catalyst has been established as the catalytic system. Both acid chlorides and anhydrides are able to acylate the benzylic position of toluene and other methylbenzenes. The method offers a valuable alternative to late transition metal catalyzed C-H acylation reactions.

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