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4-Penten-1-one, 1-cyclohexyl-2,4-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62834-91-7

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62834-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62834-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,3 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62834-91:
(7*6)+(6*2)+(5*8)+(4*3)+(3*4)+(2*9)+(1*1)=137
137 % 10 = 7
So 62834-91-7 is a valid CAS Registry Number.

62834-91-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexyl-2,4-dimethylpent-4-en-1-one

1.2 Other means of identification

Product number -
Other names 4-Penten-1-one,1-cyclohexyl-2,4-dimethyl

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:62834-91-7 SDS

62834-91-7Upstream product

62834-91-7Downstream Products

62834-91-7Relevant academic research and scientific papers

Catalyzed Reactions of Enol Ethers with SN1 Active Groups: A Novel Method for the Preparation of α-Alkylated Ketones

Gansaeuer, Andreas,Fielenbach, Doris,Stock, Christoph,Geich-Gimbel, Daniel

, p. 1017 - 1030 (2003)

The performance of tert-alkylations, alkoxyalkylations, and aldehyde enolate allylations proceeding with low catalyst loading (0.1 mol % - 5 mol %) is described. The reactions are complete within short times and can even be performed without solvent and under ambient conditions. The mechanism of the reaction was investigated by deuterium labeling and cross-over studies.

Catalyzed Reactions of Enolates and Cations: A Novel Method for Enolate Alkylation

Gansaeuer, Andreas,Fielenbach, Doris,Stock, Christoph

, p. 845 - 848 (2007/10/03)

The first tertiary alkylations, alkoxyalkylations, and aldehyde enolate allylations are described proceeding with low catalyst loading (0.1 mol % to 5 mol %). The reactions proceed in short times, can be performed without solvent and under ambient conditions.

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