142039-30-3

Basic information

• Product Name: (E)-1-(3,3-dimethylbut-1-en-1-yl)-4-methylbenzene
• Synonyms: (E)-1-(3,3-dimethylbut-1-en-1-yl)-4-methylbenzene
• CAS NO: 142039-30-3
• Molecular Weight: 174.286
• Mol File: 142039-30-3.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: (E)-1-(3,3-dimethylbut-1-en-1-yl)-4-methylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-(3,3-dimethylbut-1-en-1-yl)-4-methylbenzene(142039-30-3)
• EPA Substance Registry System: (E)-1-(3,3-dimethylbut-1-en-1-yl)-4-methylbenzene(142039-30-3)

Safety Data

• Hazardous Substances Data: 142039-30-3(Hazardous Substances Data)

Upstream product

• 624-31-7 4-tolyl iodide 
• 86595-37-1 trans-2-tert-butylvinylboronic acid 
• 630-19-3 pivalaldehyde 
• 766-97-2 4-n-methylphenylacetylene 
• 60512-56-3 1-(2,2-dibromovinyl)-4-methylbenzene 
• 677-22-5 tert-butylmagnesium chloride 
• 558-17-8 tert-Butyl iodide 
• 101671-00-5 (E)-2-(4-methylphenyl)-1-nitroethene 
• 42928-43-8 9-tert-butyl-9-borabicyclo[3.3.1]nonane 
• 74215-22-8 (3R,4S)-3-tert-Butyl-4-p-tolyl-oxetan-2-one 
• 917-64-6 methyl magnesium iodide 
• 142039-25-6 2-Methyl-2-((E)-2-p-tolyl-vinyl)-[1,3]dithiolane 
• 594-56-9 2,2,3-trimethylbut-1-ene 
• 79756-95-9 1-(3,3-dimethyl-1-butyn-1-yl)-4-methylbenzene 

Relevant articles and documents

Cu-mediated or metal-free alkylation of gem-dibromoalkenes with tertiary, secondary and primary alkyl Grignard reagents

A novel copper-mediated or transition-metal-free alkylation of gem-dibromoalkenes with tertiary, secondary and primary alkyl Grignard reagents was described. The outcomes of these reactions were found to be highly dependent on the reaction conditions and

Metal-Free Oxidative Decarbonylative Hydroalkylation of Alkynes with Secondary and Tertiary Alkyl Aldehydes

A new, metal-free, radical-mediated oxidative decarbonylative hydroalkylation of various alkynes with secondary and tertiary alkyl aldehydes using di-tert-butyl peroxide (DTBP) as oxidant is presented. This method enables the simultaneous formation of a C C bond and a C H bond through a sequence of decarbonylation, radical addition and protonation, and provides a straightforward route for transforming alkynes into alkenes with high compatibility with both alkynes and alkyl aldehydes. (Figure presented.) .

Silver-catalyzed regioselective carbomagnesiation of alkynes with alkyl halides and Grignard reagents

A silver-catalyzed carbomagnesiation of alkynes with alkyl halides and Grignard reagents afforded alkenyl Grignard reagents regioselectively, where the alkyl group of the alkyl halide, but not that of the Grignard reagent, was introduced into the alkyne.