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116408-27-6

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116408-27-6 Usage

Type of Compound

Long-chain hydrocarbon

Classification

Unsaturated fatty acid

Subtype

Polyunsaturated fat

Double Bonds

Two double bonds located at the ninth and tenth carbon atoms

Configuration

(Z)-9,10-Octadecadiene, indicating the cis configuration of the double bonds

Natural Sources

Commonly found in vegetable oils

Industrial Applications

Used as a precursor for the synthesis of fragrances, flavorings, and polymer materials

Research Applications

Potential applications in the field of chemistry research

Chemical Intermediate

Used for the production of other compounds

Check Digit Verification of cas no

The CAS Registry Mumber 116408-27-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,0 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 116408-27:
(8*1)+(7*1)+(6*6)+(5*4)+(4*0)+(3*8)+(2*2)+(1*7)=106
106 % 10 = 6
So 116408-27-6 is a valid CAS Registry Number.

116408-27-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name octadeca-1,9-diene

1.2 Other means of identification

Product number -
Other names 1,9-Octadecadiene

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:116408-27-6 SDS

116408-27-6Upstream product

116408-27-6Relevant articles and documents

Pheromones via organoboranes: Part IV - Synthesis of (Z)-9-tricosene (Muscalure)

Dhillon, Ranjit S.,Singh, Rupinder P.,Singh, Jasvinder

, p. 718 - 721 (2007/10/03)

Synthesis of (Z)-9-tricosene (muscalure) (9) is reported starting from oleyl alcohol by two carbon homologation via dianion of phenoxyacetic acid followed by reduction (LAH), oxidation (PCC) and Grignard reaction.

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