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Cyclohexanone, 2-[(dimethylamino)methyl]-6-(phenylmethylene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57754-23-1

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57754-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57754-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,5 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57754-23:
(7*5)+(6*7)+(5*7)+(4*5)+(3*4)+(2*2)+(1*3)=151
151 % 10 = 1
So 57754-23-1 is a valid CAS Registry Number.

57754-23-1SDS

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 2-benzylidene-6-[(dimethylamino)methyl]cyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 2-Dimethylaminomethyl-6-benzylidencyclohexan

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:57754-23-1 SDS

57754-23-1Downstream Products

57754-23-1Relevant academic research and scientific papers

Intramolecular cyclization of alicyclic 1,5-di-and 1,3,5-triketones

Akimova,Ivanenko,Vysotskii

, p. 1068 - 1073 (2001)

On a series of 44 alicyclic 1,5-di-and 1,3,5-triketones was studied the influence of various structural factors (size of the 5-7-membered ring, positions of the substituents) on the capability for intramolecular aldol condensation and on its direction. The most prone to this reaction are compounds possessing a 6-membered cycle and a substituent in the β-methylene bridge. The substituent in α-position to one of the carbonyl groups can affect the reaction in two ways depending on the degree of shielding of this position.

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