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Ethanone, 2-chloro-1-(4-chlorophenyl)-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65240-71-3

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65240-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65240-71-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,4 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65240-71:
(7*6)+(6*5)+(5*2)+(4*4)+(3*0)+(2*7)+(1*1)=113
113 % 10 = 3
So 65240-71-3 is a valid CAS Registry Number.

65240-71-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-(4-chlorophenyl)-2-phenylethanone

1.2 Other means of identification

Product number -
Other names p-Chlor-α-chlor-deoxybenzoin

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:65240-71-3 SDS

65240-71-3Upstream product

65240-71-3Relevant academic research and scientific papers

Utilization of natural sunlight and air in the aerobic oxidation of benzyl halides

Su, Yijin,Zhang, Liangren,Jiao, Ning

supporting information; body text, p. 2168 - 2171 (2011/06/21)

Chemical equations presented. A novel, efficient oxidation of α-aryl halogen derivatives to the corresponding α-aryl carbonyl compounds at room temperature has been disclosed. Natural sunlight and air are successfully utilized in this approach through the combination of photocatalysis and organocatalysis. A plausible mechanism was proposed on the basis of the mechanistic studies.

"STRUCTURE-REACTIVITY-SELECTIVITY" RELATIONSHIP IN SN2 PROCESSES. REACTION OF 4,4'-SUBSTITUTED α-CHLORODEOXYBENZOINS WITH SODIUM THIOPHENOLATES

Karavan, V. S.,Simonov, D. A.

, p. 145 - 148 (2007/10/02)

In the SN2 reactions of α-chlorodeoxybenzoins X'C6H4CHClCOC6H4X with YC6H4SNa in methanol there is no unambiguous relationship at all between the reactivity of the substrate and its selectivity toward the nucleophile (ρY).At the same

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