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

76886-47-0

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76886-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76886-47-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,8 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76886-47:
(7*7)+(6*6)+(5*8)+(4*8)+(3*6)+(2*4)+(1*7)=190
190 % 10 = 0
So 76886-47-0 is a valid CAS Registry Number.

76886-47-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohexylidenemethyl-diisopropylamine

1.2 Other means of identification

Product number -
Other names -

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:76886-47-0 SDS

76886-47-0Relevant academic research and scientific papers

Generation of Aldehydic Enol Ethers and Enamines by Olefination of Ketones

Gilbert, John C.,Weerasooriya, Upali

, p. 448 - 453 (2007/10/02)

Reaction of aliphatic ketones with dimethyl (diazomethyl)phosphonate (5, R = CH3) in the presence of alcohols and amines afforded enol ethers and enamines, respectively, of the next higher aldehyde.The technique has been found to be applicable to several

A NOVEL ROUTE TO ALDEHYDIC ENOL ETHERS AND ENAMINES

Gilbert, J. C.,Weerasooriya, U.

, p. 2041 - 2044 (2007/10/02)

Base-promoted reaction of dimethyl diazomethylphosphonate (1) with dialkyl and cyclic ketones in the presence of alcohols and of amines affords aldehydic enol ethers and enamines, respectively.

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