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68043-00-5

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68043-00-5 Usage

Chemical compound

3-Methyl-2-(2-pentenyl)-2-cyclopentene-1-one

Molecular structure

Contains a cyclopentene ring

Components

Methyl group, pentenyl group, cyclopentene-1-one group

Applications

Used in pharmaceutical and industrial applications

Properties

Studied for potential biological and chemical properties

Versatile

Can be used in organic synthesis and as a building block in chemical compound production

Potential

Suitable for development of new drugs and materials based on its unique molecular structure and functional groups.

Check Digit Verification of cas no

The CAS Registry Mumber 68043-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,4 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 68043-00:
(7*6)+(6*8)+(5*0)+(4*4)+(3*3)+(2*0)+(1*0)=115
115 % 10 = 5
So 68043-00-5 is a valid CAS Registry Number.

68043-00-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-2-pent-2-enylcyclopent-2-en-1-one

1.2 Other means of identification

Product number -
Other names cis-Jasmon

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:68043-00-5 SDS

68043-00-5Downstream Products

68043-00-5Relevant articles and documents

Synthesis of cis-Jasmone via the Retroaldol-aldol Condensation of 3-(cis-3-hexenyl)-2-cyclopentenone in an Autoclave

Yoshida, Takashi,Saito, Shojiro

, p. 3931 - 3932 (2007/10/02)

cis-Jasmone was efficiently synthesized from 2-cyclopentenone.The treatment of cyclopentenone with sodium p-toluenesulfinate gave 3-(p-tolylsulfonyl)cyclopentanone in a 92.5percent yield.The alkylation of the sulfone, after the protection of the ketone, with cis-1-bromo-3-hexene, followed by desulfonylation with 5percent hydrochloric acid in tetrahydrofuran, afforded 3-(cis-3-hexenyl)-2-cyclopentenone in a good yield.The retroaldol-aldol condensation of the cyclopentenone in a stainless steel autoclave in presence of 5percent sodium hydroxide yielded cis-jasmone in a 80percent yield.

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