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22433-34-7

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22433-34-7 Usage

General Description

2,3-Nonadiene, also known as divinyl, is a colorless flammable liquid with a faint odor. It is a hydrocarbon with the chemical formula C9H16 and exists as two isomers: 2,3-trans-nonadiene and 2,3-cis-nonadiene. 2,3-Nonadiene is primarily used as a monomer in the production of various polymers and resins, such as polyethylene and polypropylene. It is also utilized in the synthesis of fragrances, adhesives, and rubber products. Additionally, 2,3-nonadiene can undergo various chemical reactions, including addition reactions, to form different derivatives and products with a wide range of applications in the chemical and manufacturing industries. However, it is important to handle this chemical with care due to its flammability and potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 22433-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,3 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22433-34:
(7*2)+(6*2)+(5*4)+(4*3)+(3*3)+(2*3)+(1*4)=77
77 % 10 = 7
So 22433-34-7 is a valid CAS Registry Number.

22433-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name nona-2,3-diene

1.2 Other means of identification

Product number -
Other names 2,3-Nonadiene

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:22433-34-7 SDS

22433-34-7Upstream product

22433-34-7Relevant articles and documents

Iron-catalyzed regio- and stereoselective carbolithiation of Alkynes

Hojo, Makoto,Murakami, Yoshio,Aihara, Hidenori,Sakuragi, Rie,Baba,Hosomi, Akira

, p. 621 - 623 (2007/10/03)

Butylation problems ironed out: 3-Pentynyl ethers react with butyllithium at - 20°C in toluene, upon addition of a catalytic amount of a cheap iron(III) salt, to afford (E)-4-methyl-3-octenyl ethers in high yields. Stereochmically defined tetrasubstituted alkenes were also obtained by the subsequent addition of electrophiles (E+, see scheme; acac = acetylacetonate, Bn = benzyl).

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