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1,5-Hexadiene, 3-ethenyl-, also known as 3-vinyl-1,5-hexadiene, is an organic compound with the chemical formula C8H12. It is a colorless liquid with a strong, pungent odor. This diene is a conjugated diene, meaning it has two carbon-carbon double bonds separated by a single bond, which allows for various chemical reactions such as Diels-Alder reactions. It is used as a monomer in the production of polymers and as a building block in the synthesis of other organic compounds. Due to its reactivity, it is typically handled under controlled conditions to prevent unwanted side reactions.

997-74-0

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997-74-0 Usage

Physical state

Colorless, flammable liquid

Usage

a. Monomer in the production of polymers
b. Production of synthetic rubbers
c. Manufacture of industrial products (adhesives, coatings, sealants)

Reactivity

Highly reactive compound

Chemical reactions

Can undergo polymerization and addition reactions

Health and environmental hazards

Potential hazards require proper handling and storage

Safety and regulatory compliance

Necessary to ensure safety and compliance with regulations

Check Digit Verification of cas no

The CAS Registry Mumber 997-74-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,9 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 997-74:
(5*9)+(4*9)+(3*7)+(2*7)+(1*4)=120
120 % 10 = 0
So 997-74-0 is a valid CAS Registry Number.

997-74-0SDS

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 3-allyl-1,4-pentadiene

1.2 Other means of identification

Product number -
Other names 3-vinyl-hexa-1,5-diene

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:997-74-0 SDS

997-74-0Upstream product

997-74-0Downstream Products

997-74-0Relevant academic research and scientific papers

Chemistry of Dienyl Anions. II. Crystalline Bis(dienyl)magnesium. Selective Dienylation and Structure in Solution and in the Solid State

Yasuda, Hajime,Yamauchi, Michihide,Nakamura, Akira,Sei, Tsuyoshi,Kai, Yasushi,et al.

, p. 1089 - 1100 (1980)

Seven different crystalline bis(dienyl)magnesium TMEDA complexes of open chain or cyclic structure were prepared by metal exchange reaction of corresponding potassium dienides.They are fluxional in solution due to the rapid 1,3-rearrangement.Terminally ?-bonded trans or (E) structure exists primarily in the open chain complexes while centrally ?-bonded cis structure in cyclic dienylmagnesium TMEDA complexes.The former gave 1,3-dienes exclusively but the latter gave 1,4-dienes upon hydrolysis.Molecular structure of bis(2,4-dimethyl-2,4-pentadienyl)magnesium determined by X-ray crystallography showed that it has terminally ?-bonded structure.Addition of dienylmagnesium compounds to acetone followed by hydrolysis gave 1,4-diene derivatives regioselectively but that to diisopropyl ketone gave 1,3-diene derivatives selectively.Unsaturated alcihols with an elongated carbon chain were synthesized by thermal cracking of cyclic ether complexes. 1,3,7-Trienes can be obtained selectively by reaction of appropriate allyl halides in the presence of CuCl catalyst and regiosective dienylation occured by using TiCl2(η5-C5H5)2 as catalyst.

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