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4-METHYLCYCLOHEXYLFORMATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40392-31-2

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40392-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40392-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,9 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40392-31:
(7*4)+(6*0)+(5*3)+(4*9)+(3*2)+(2*3)+(1*1)=92
92 % 10 = 2
So 40392-31-2 is a valid CAS Registry Number.

40392-31-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylcyclohexane-1-carboxylate

1.2 Other means of identification

Product number -
Other names 4-METHYLCYCLOHEXYLFORMATE

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:40392-31-2 SDS

40392-31-2Downstream Products

40392-31-2Relevant academic research and scientific papers

Efficient catalytic reduction of ketones with formic acid and ruthenium complexes

Menashe, Naim,Salant, Einat,Shvo, Youval

, p. 97 - 102 (2007/10/03)

The ruthenium complex (η5-C4Ph4COHOC4Ph4-η5)( μ-H)(CO)4Ru2 and its phenyl ring-substituted derivatives were found to act as efficient catalysts in reduction reactions of aldehydes and ketones to alcohols, using formic acid as H source. Excess formic acid accelerates the reaction, and the corresponding formate esters were isolated as sole products. Turnover numbers of up to 8000 (alcohols) and 11000 (formate esters) were attained, with yields in the order of 90%. Alkenes are not reactive, however, double bonds conjugated to a carbonyl group are selectively reduced under the reaction conditions. The reaction is compatible with a variety of ketones, but with aliphatic aldehydes the reaction is not selective, inasmuch as aldol condensation products are formed.

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