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Ethanone, 1-cyclohexyl-2-cyclohexylidene- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62939-75-7

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62939-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62939-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,3 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62939-75:
(7*6)+(6*2)+(5*9)+(4*3)+(3*9)+(2*7)+(1*5)=157
157 % 10 = 7
So 62939-75-7 is a valid CAS Registry Number.

62939-75-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexyl-2-cyclohexylideneethanone

1.2 Other means of identification

Product number -
Other names Ethanone,1-cyclohexyl-2-cyclohexylidene

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:62939-75-7 SDS

62939-75-7Downstream Products

62939-75-7Relevant academic research and scientific papers

Gold-catalyzed efficient formation of α,β-unsaturated ketones from propargylic acetates

Yu, Meng,Li, Guotao,Wang, Shaozhong,Zhang, Liming

, p. 871 - 875 (2007)

An efficient gold-catalyzed method for the preparation of α,β-unsaturated ketones from propargylic acetates has been developed. Under mild reaction conditions, β-monosubstituted enones were formed mostly with excellent E-selectivity. β,β-Disubstituted enones can be prepared from propargylic acetates derived from ketones. The high efficiency and mild nature of this reaction render it a viable alternative for the synthesis of α,β-unsaturated ketones.

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