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82937-00-6

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82937-00-6 Usage

Description

(4Z)-2,4-dimethylhexa-2,4-diene is a chemical compound with the molecular formula C8H14. It is an unsaturated hydrocarbon, specifically a diene, meaning it contains two double bonds in its carbon chain. The "4Z" designation indicates that the double bonds are in a cis configuration, with both methyl groups on the same side of the molecule. (4Z)-2,4-dimethylhexa-2,4-diene is known for its versatility and importance in organic synthesis due to its physical and chemical properties.

Uses

Used in Organic Synthesis:
(4Z)-2,4-dimethylhexa-2,4-diene is used as a synthetic intermediate for the production of various chemical compounds. Its unique structure with two double bonds in a cis configuration allows for a wide range of reactions and transformations, making it a valuable building block in the synthesis of complex organic molecules.
Used in Polymer Production:
(4Z)-2,4-dimethylhexa-2,4-diene is also utilized in the production of different types of polymers. Its ability to undergo polymerization reactions contributes to the creation of polymers with specific properties, such as strength, flexibility, and durability, which are essential in various industries.
Used in Pharmaceutical Industry:
(4Z)-2,4-dimethylhexa-2,4-diene can be used as a starting material for the synthesis of pharmaceutical compounds. Its reactivity and structural features make it suitable for the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
Due to its unique structure and reactivity, (4Z)-2,4-dimethylhexa-2,4-diene is often employed in chemical research to study various reaction mechanisms, explore new synthetic routes, and develop innovative methodologies in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 82937-00-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,3 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82937-00:
(7*8)+(6*2)+(5*9)+(4*3)+(3*7)+(2*0)+(1*0)=146
146 % 10 = 6
So 82937-00-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H14/c1-5-8(4)6-7(2)3/h5-6H,1-4H3/b8-5-

82937-00-6SDS

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 2,4-dimethylhexa-2,4-diene

1.2 Other means of identification

Product number -
Other names E-2,4-dimethyl-2,4-hexadiene

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:82937-00-6 SDS

82937-00-6Relevant articles and documents

Cyclobutene photochemistry. Involvement of carbene intermediates in the photochemistry of alkylcyclobutenes

Clark, K. Brady,Leigh, William J.

, p. 1571 - 1578 (2007/10/02)

The photochemistry of 1,3,3,4- and 1,3,4,4-tetramethylcyclobutene has been investigated in pentane solution with monochromatic far ultraviolet (185, 193, and 214nm) light sources, as well as in methanol solution with 214-nm excitation.Photolysis of each of the two isomeric cyclobutene derivatives results in competitive electrocyclic ring opening (yielding mixtures of stereoisomeric dienes in each case), fragmentation to yield propyne and methyl-2-butene, and isomerization to the other cyclobutene isomer.Quantum yields for product formation with 185-nm excitation have been measured in each case by cyclooctene actinometry.The occurrence of the interconversion process is offered as evidence for the intermediacy of cyclopropyl carbenes in the photochemistry of simple cyclobutenes in solution.On the basis of the known chemistry of carbenes of this type, their intermediacy in cyclobutene photochemistry may account at least partially for the formation of the formal (2?+2?) cycloreversion products from photolysis of simple cyclobutene derivatives.

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