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26294-59-7

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26294-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26294-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,9 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 26294-59:
(7*2)+(6*6)+(5*2)+(4*9)+(3*4)+(2*5)+(1*9)=127
127 % 10 = 7
So 26294-59-7 is a valid CAS Registry Number.

26294-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-6-(4-methylcyclohex-3-en-1-yl) hepta-2,5-dien-4-one

1.2 Other means of identification

Product number -
Other names 2-methyl-6-((R)-4-methyl-cyclohex-3-enyl)-hepta-2,5c-dien-4-one

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:26294-59-7 SDS

26294-59-7Relevant academic research and scientific papers

Synthese de cetones a partir de N-phenyl imidothioesters et par l'intermediaire de cetenimines

El-Jazouli, Mustapha,Lage, Nadia,Masson, Serge,Thuillier, Andre

, p. 883 - 888 (2007/10/02)

The thermal decomposition of metallated N-phenyl imidothioesters (lithium or magnesium alkylthio-enaminates generated by either deprotonation or 1,4-addition) led to ketenimines which were trapped in situ by organo-lithium or magnesium compounds to give metallated imines, readily hydrolysed into ketones.This sequence allowed the use of imidothioesters as acyl cation equivalents and also successive and regioselective > 1,3-additions of two different organometallics to an α-unsaturated imidothioester.Ar-turmerone, 2,6-dimethyl-2,7-octadien-4-one, iso-artemisia ketone, α-atlantone and other unsymmetrical ketones were synthesized by this procedure.

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