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Cyclohexanone, 3-ethenyl-3-methyl-4-(1-methylethenyl)-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30824-87-4

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30824-87-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30824-87-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,8,2 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30824-87:
(7*3)+(6*0)+(5*8)+(4*2)+(3*4)+(2*8)+(1*7)=104
104 % 10 = 4
So 30824-87-4 is a valid CAS Registry Number.

30824-87-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-Desisopropyliden-β-elemenon

1.2 Other means of identification

Product number -
Other names trans-1,2-Divinylcyclohexanon

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:30824-87-4 SDS

30824-87-4Relevant academic research and scientific papers

TOTAL SYNTHESIS OF VARIOUS ELEMANOLIDES

Friedrich, Dirk,Bohlmann, Ferdinand

, p. 1369 - 1392 (2007/10/02)

Starting with a suitable substituted divinyl cyclohexanone, eleven naturally occurring 12.8-elemanolides bearing exo-methylene or methyl groups at C-11 and differing in substitution as well as in relative configuration, have been synthesized in racemic form.An approach to elemanolides with additional oxygen functionalities is principally possible by modification of the basic concept.Methods for the oxidative generation of terpenoid exo-methylene lactone and furan units are exemplified by synthesis of menthofuran and the p-menthenolides from isopulegols.

A NEW FORMAL TOTAL SYNTHESIS OF β-ELEMENONE

Soria, O.,Maldonado, L. A.

, p. 1093 - 1097 (2007/10/02)

A short, stereoselective synthesis of an intermediate in Grieco's synthesis of β-elemenone is described

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