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5587-77-9

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5587-77-9 Usage

Structure

Long-chain alcohol with a cyclopentene ring

Field of use

Organic chemistry

Applications

Synthetic reactions, precursor for other organic compounds

Industry relevance

Pharmaceutical, fragrance, and fine chemical production

Potential applications

Development of new materials and biologically active compounds

Check Digit Verification of cas no

The CAS Registry Mumber 5587-77-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,8 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5587-77:
(6*5)+(5*5)+(4*8)+(3*7)+(2*7)+(1*7)=129
129 % 10 = 9
So 5587-77-9 is a valid CAS Registry Number.

5587-77-9SDS

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 11-cyclopent-2-en-1-ylundecan-1-ol

1.2 Other means of identification

Product number -
Other names (+)-Hydnocarpylalkohol

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:5587-77-9 SDS

5587-77-9Downstream Products

5587-77-9Relevant articles and documents

ASYMMETRIC SYNTHESIS OF CHIRAL COMPOUNDS

-

, (2015/02/02)

The present invention provides processes for the production of chiral compounds in a stereoisomeric excess, the processes comprising: (i) contacting a first compound comprising an alkene or alkyne bond with a hydrometallating agent, wherein the first compound and the hydrometallating agent are contacted under conditions such that the first compound is hydrometallated by said hydrometallating agent; and (ii) contacting the hydrometallated first compound with a second compound comprising an allylic group, wherein the hydrometallated first compound and the second compound are contacted under conditions such that they undergo an asymmetric allylic alkylation reaction in which a carbon atom of the hydrometallated first compound binds to a carbon atom of said allylic group, forming a stereoisomeric excess of a compound having a chiral centre in an allylic position, said chiral centre being located at the carbon atom bound by said first compound, wherein said asymmetric allylic alkylation reaction is performed in the presence of a metal catalyst comprising a chiral ligand. In particular, the present invention provides processes for the production of a stereoisomeric excess of a compound of the formula (IA), (IB), (IA') or (IB') as defined herein.

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