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α-Benzoyldiphenylmethyl chloride, also known as α-benzoyldiphenylmethyl chloride or 1-(benzoyloxy)-1-diphenylmethyl chloride, is an organic compound with the chemical formula C20H17ClO. It is a white crystalline solid that is soluble in organic solvents. α-benzoyldiphenylmethyl chloride is a derivative of diphenylmethyl chloride, featuring a benzoyl group attached to the carbon atom. It is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds due to its reactivity and stability. The presence of the benzoyl group makes it a valuable building block for the preparation of complex molecules, particularly in the field of medicinal chemistry.

2510-77-2

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2510-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2510-77-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,1 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2510-77:
(6*2)+(5*5)+(4*1)+(3*0)+(2*7)+(1*7)=62
62 % 10 = 2
So 2510-77-2 is a valid CAS Registry Number.

2510-77-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name α-benzoyldiphenylmethyl chloride

1.2 Other means of identification

Product number -
Other names 2-chloro-1,2,2-triphenylethan-1-one

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:2510-77-2 SDS

2510-77-2Relevant academic research and scientific papers

Photorelease study of γ-amino glutamate from 1,2,2-triphenyl-ethanone

Jang, Sukjin,Chowdhury, Azhad,Kang, Jeonghee,Lee, Jong I.

, p. 230 - 235 (2014/05/20)

A phototrigger, 1,2,2-triphenylethanone (TPE), was synthesized for the photorelease study. The photorelease of 1,2,2-triphenylethanonyl N-t-Boc-γ-amino glutamate (TPE- N-t-Boc-GABA) showed the quantum efficiency of φ = 0.75. The phototrigger underwent fur

2-Hydroxy-1,2,2-triphenylethanone as an efficient photolabile protecting group for carboxylic acids

Ashraf, M. Arfan,Russell, Alexander G.,Wharton, Christopher W.,Snaith, John S.

, p. 586 - 593 (2007/10/03)

The synthesis is reported of 2-hydroxy-1,2,2-triphenylethanone esters of carboxylic acids by the reaction between 2-chloro-1,2,2-triphenylethanone and a carboxylic acid in the presence of silver carbonate and silver tetrafluoroborate. Photolysis of the esters occurs rapidly on irradiation with a medium-pressure mercury lamp through quartz or Pyrex to return the carboxylic acid. The side product of the photolysis is benzo[b]phenanthro[9,10-d]furan, formed through a tandem process involving initial generation of 2,3-diphenylbenzofuran, photochemical cyclisation and re-aromatisation by aerial oxidation.

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