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2,6-bis[(dimethylamino)methyl]cyclohexanone is a complex organic compound with the molecular formula C13H27NO2. It is a derivative of cyclohexanone, featuring two dimethylamino groups attached to the 2nd and 6th carbon atoms of the cyclohexane ring, with a methyl group extending from each nitrogen atom. 2,6-bis[(dimethylamino)methyl]cyclohexanone is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a precursor in the production of certain pesticides. Its structure endows it with unique chemical properties, making it a valuable intermediate in organic synthesis.

2478-21-9

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2478-21-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2478-21-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,7 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2478-21:
(6*2)+(5*4)+(4*7)+(3*8)+(2*2)+(1*1)=89
89 % 10 = 9
So 2478-21-9 is a valid CAS Registry Number.

2478-21-9SDS

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 2,6-bisdimethylaminomethylcyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 2,6-Bis-dimethylaminomethyl-cyclohexanone

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

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More Details:2478-21-9 SDS

2478-21-9Relevant academic research and scientific papers

Methods of synthesis of alicyclic 1,5,9-triketones. Reaction of transaminomethylation

Akimova,Soldatkina,Ivanenko, Zh. A.,Savchenko

, p. 720 - 728 (2017/07/07)

Alicyclic 1,5,9-triketones with various combination of 5-, 6-, 7-membereded cycles in the molecule were obtained by methods of diketone condensation, Michael reaction, and proceeding from Mannich mono- and bisbases and cycloalkanones. The latter method wa

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