82937-01-7

Basic information

• Product Name: (4E)-2,4-dimethylhexa-2,4-diene
• CAS NO: 82937-01-7
• Molecular Formula: C₈H₁₄
• Molecular Weight: 110.1968
• Mol File: 82937-01-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 127.5°C at 760 mmHg
• Flash Point: 17.1°C
• Density: 0.747g/cm³
• Vapor Pressure: 13.5mmHg at 25°C
• Refractive Index: 1.44
• CAS DataBase Reference: (4E)-2,4-dimethylhexa-2,4-diene(CAS DataBase Reference)
• NIST Chemistry Reference: (4E)-2,4-dimethylhexa-2,4-diene(82937-01-7)
• EPA Substance Registry System: (4E)-2,4-dimethylhexa-2,4-diene(82937-01-7)

Safety Data

• Hazardous Substances Data: 82937-01-7(Hazardous Substances Data)

Upstream product

• 674-82-8 4-methyleneoxetan-2-one 
• 1569-43-3 3,5-dimethyl-hex-4-en-3-ol 
• 121-44-8 triethylamine 
• 10467-10-4 ethylmagnesium iodide 
• 141-79-7 4-methyl-pent-3-en-2-one 
• 60-29-7 diethyl ether 
• 85-44-9 phthalic anhydride 
• 29649-22-7 2,4-dimethyl-hexane-2,4-diol 
• 1569-46-6 2,4-Dimethyl-hexen-(1)-ol-(4) 
• 1530-32-1 ethyltriphenylphosphonium bromide 
• 82937-00-6 (Z)-2,4-Dimethyl-2,4-hexadiene 
• 42302-74-9 2,2,4-trimethyl-3-pentanal p-tozylhydrazonate 
• 116851-49-1 1,3,3,4-tetramethylcyclobutene 
• 503-17-3 dimethylacetylene 

Downstream Products

• 856633-44-8 2,3-dimethyl-2-(2-methyl-propenyl)-oxirane 
• 103985-59-7 acetic acid-(4-hydroxy-1,1,3-trimethyl-pent-2-enyl ester) 
• 589-43-5 2,4-dimethylhexane 

Relevant articles and documents

A new [2 + 2] functionalization of C60 with alkyl-substituted 1,3- butadienes: A mechanistic approach. Stereochemistry and isotope effects

The stereochemistry and secondary isotope effects of the [2 + 2] photocycloaddition of trans,trans- (7), cis,cis- (8), and cis,trans-2,4- hexadiene (9), 2,5-dimethyl-2,4-hexadiene (1), and its deuterated analogues 1-d1, 1-d6, and tra

A FACILE HIGH-YIELD SYNTHESIS OF DI-η5-CYCLOPENTADIENYLHAFNACYCLOPENTADIENE COMPOUNDS

Hafnocene dichloride was reduced with amalgamated magnesium in the presence of alkynes giving high yields of di-η5-cyclopentadienylhafnacyclopentadienes.Reaction with hydrochloric acid yields exclusively the corresponding (E,E)-butadiene deriva