82937-00-6

Basic information

• Product Name: (4Z)-2,4-dimethylhexa-2,4-diene
• Synonyms: (4Z)-2,4-dimethylhexa-2,4-diene
• CAS NO: 82937-00-6
• Molecular Formula: C₈H₁₄
• Molecular Weight: 110.2
• Mol File: 82937-00-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 127.5°C at 760 mmHg
• Flash Point: 17.1°C
• Appearance: /
• Density: 0.747g/cm³
• Vapor Pressure: 13.5mmHg at 25°C
• Refractive Index: 1.44
• CAS DataBase Reference: (4Z)-2,4-dimethylhexa-2,4-diene(CAS DataBase Reference)
• NIST Chemistry Reference: (4Z)-2,4-dimethylhexa-2,4-diene(82937-00-6)
• EPA Substance Registry System: (4Z)-2,4-dimethylhexa-2,4-diene(82937-00-6)

Safety Data

• Hazardous Substances Data: 82937-00-6(Hazardous Substances Data)

Usage

General 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 commonly used as a synthetic intermediate in organic chemistry, and it is often employed in the production of various polymers and chemical compounds. The physical and chemical properties of (4Z)-2,4-dimethylhexa-2,4-diene make it a versatile and important compound in the field of organic synthesis.

InChI:InChI=1/C8H14/c1-5-8(4)6-7(2)3/h5-6H,1-4H3/b8-5-

Upstream product

• 116851-49-1 1,3,3,4-tetramethylcyclobutene 
• 42302-74-9 2,2,4-trimethyl-3-pentanal p-tozylhydrazonate 
• 141-79-7 4-methyl-pent-3-en-2-one 
• 1530-32-1 ethyltriphenylphosphonium bromide 

Downstream Products

• 82937-01-7 (E)-2,4-dimethyl-hexa-2,4-diene 

Relevant articles and documents

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

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.