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10482-53-8

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10482-53-8 Usage

General Description

(Z,Z,Z)-heptadeca-1,8,11,14-tetraene is a chemical compound with the molecular formula C17H24 and a systematic name of 1,8,11,14-heptadecatetraene. It is an organic compound that belongs to the class of polyunsaturated hydrocarbons, specifically a type of acyclic hydrocarbon known as a polyene. (Z,Z,Z)-heptadeca-1,8,11,14-tetraene contains a chain of 17 carbon atoms with alternating double bonds, giving it a linear structure. The presence of multiple double bonds makes it highly reactive and capable of participating in various chemical reactions. (Z,Z,Z)-heptadeca-1,8,11,14-tetraene may be used in organic synthesis or chemical research as a starting material or intermediate for the production of other complex compounds. However, it should be handled with caution due to its potential reactivity and flammability.

Check Digit Verification of cas no

The CAS Registry Mumber 10482-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,8 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10482-53:
(7*1)+(6*0)+(5*4)+(4*8)+(3*2)+(2*5)+(1*3)=78
78 % 10 = 8
So 10482-53-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H28/c1-3-5-7-9-11-13-15-17-16-14-12-10-8-6-4-2/h3,6,8,12,14-15,17H,1,4-5,7,9-11,13,16H2,2H3/b8-6-,14-12-,17-15-

10482-53-8SDS

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 (8Z,11Z,14Z)-heptadeca-1,8,11,14-tetraene

1.2 Other means of identification

Product number -
Other names Heptadecatetraen

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:10482-53-8 SDS

10482-53-8Downstream Products

10482-53-8Relevant articles and documents

ISOLATION AND TOTAL SYNTHESIS OF THE MAJOR CONSTITUENT OF THE ROOTS OF CENTAUREA INCANA: APLOTAXENE

Cossy, J.,Aclinou, P.

, p. 7615 - 7618 (1990)

The major constituent of the petroleum ether extract of the root of Centaurea incana was identified as (8Z,11Z,14Z)-1,8,11,14-heptadecatetraene (Aplotaxene 1).A convergent and highly stereoselective synthesis of this compound is reported.

Amines as effective ligands in iridium-catalyzed decarbonylative dehydration of biosourced substrates

Ternel, Jérémy,Léger, Bastien,Monflier, Eric,Hapiot, Frédéric

, p. 3948 - 3953 (2018)

Linear α-olefins (LAOs) and linear internal olefins (LIOs) are essential intermediates in the synthesis of surfactants, lubricants, and polymers. Concurrently with petroleum-based industrial processes, the production of LAOs and LIOs from renewable feedstocks has gained increasing interest in recent years. Organometallic catalysts have been developed designedly, especially Pd, Fe and Ir catalysts. However, such catalysts are mostly stabilized by phosphanes, ligands sometimes difficult to handle especially on large scales. Alternatives to phosphanes would thus be highly desirable. In the present study, we demonstrate that Ir catalysts coordinated by amines are suitable to decarbonylate a wide range of biosourced substrates under mild conditions. The resulting LAOs and LIOs are obtained with good conversion provided that the nature and the quantity of the amines are controlled accurately. The LAO/LIO selectivity can also be tuned by a judicious choice of experimental conditions. Interestingly, the Ir-based catalytic system is applicable to the decarbonylative dehydration of saturated, unsaturated and polyunsaturated fatty acids.

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