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Cyclohexanone, 2-[(2-chlorophenyl)methyl]-, also known as 1-(2-chlorobenzyl)cyclohexanone, is an organic compound with the molecular formula C13H15ClO. It is a colorless to pale yellow liquid with a molecular weight of 222.7 g/mol. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is characterized by its unique structure, which consists of a cyclohexanone ring with a 2-chlorophenylmethyl group attached to the 2-position. Due to its reactivity and versatility, it is an important building block in the chemical industry, enabling the production of a wide range of products with diverse applications.

2702-77-4

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2702-77-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2702-77-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,0 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2702-77:
(6*2)+(5*7)+(4*0)+(3*2)+(2*7)+(1*7)=74
74 % 10 = 4
So 2702-77-4 is a valid CAS Registry Number.

2702-77-4SDS

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-[2-Chlor-benzyl]-cyclohexanon

1.2 Other means of identification

Product number -
Other names 2-(2-Chlor-benzyl)-cyclohexanon

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:2702-77-4 SDS

2702-77-4Relevant academic research and scientific papers

β-Arylation of oxime ethers using diaryliodonium salts through activation of inert C(sp 3)-H bonds using a palladium catalyst

Peng, Jing,Chen, Chao,Xi, Chanjuan

, p. 1383 - 1387 (2016)

An efficient method of selective β-arylation of oxime ethers was realized by using a palladium catalyst with diaryliodonium salts as the key arylation reagents. The reaction proceeded smoothly through the activation of inert C(sp3)-H bonds to give corresponding ketones and aldehydes. This convenient procedure can be successfully applied to construct new C(sp3)-C(sp2) bonds on a number of complex molecules derived from natural products and thus serves as a practical synthetic tool for direct late-stage C(sp3)-H functionalization.

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