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1(3aH)-Pentalenone,4,5,6,6a-tetrahydro-3,6-dimethyl-,(3aR,6S,6aS)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

343930-24-5

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  • 1(3aH)-Pentalenone,4,5,6,6a-tetrahydro-3,6-dimethyl-,(3aR,6S,6aS)-(9CI)

    Cas No: 343930-24-5

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343930-24-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 343930-24-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,3,9,3 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 343930-24:
(8*3)+(7*4)+(6*3)+(5*9)+(4*3)+(3*0)+(2*2)+(1*4)=135
135 % 10 = 5
So 343930-24-5 is a valid CAS Registry Number.

343930-24-5SDS

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 (3aR,6S,6aS)-3,6-Dimethyl-4,5,6,6a-tetrahydro-3aH-pentalen-1-one

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:343930-24-5 SDS

343930-24-5Downstream Products

343930-24-5Relevant articles and documents

Enantioselective total syntheses of the novel tricyclic sesquiterpene hydrocarbons (+)- and (-)-kelsoene. Absolute configuration of the natural product

Mehta, Goverdhan,Srinivas

, p. 2855 - 2857 (2007/10/03)

Simple and preparatively efficacious lipase-catalysed kinetic resolution of endo,endo-cis-bicyclo[3.3.0]octane-2,6-diol rac-3 has provided ready access to bicyclo[3.3.0]octane-2,6-diones (-)-2 and (+)-2 of high enantiomeric purity. These C2-symmetric diones have been further elaborated to the sesquiterpene hydrocarbon (+)-kelsoene 1 and ent-kelsoene (-)-1, respectively, thereby establishing the absolute configuration of the natural product. In the light of these results, the absolute configuration assigned earlier to (+)-kelsoene needs to be revised as (+)-1.

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