4333-55-5

Basic information

• Product Name: Benzene, 1,1'-(1-propenylidene)bis[4-methyl-
• CAS NO: 4333-55-5
• Molecular Formula: C17H18
• Molecular Weight: 222.33
• Mol File: 4333-55-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-(1-propenylidene)bis[4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-(1-propenylidene)bis[4-methyl-(4333-55-5)
• EPA Substance Registry System: Benzene, 1,1'-(1-propenylidene)bis[4-methyl-(4333-55-5)

Safety Data

• Hazardous Substances Data: 4333-55-5(Hazardous Substances Data)

Upstream product

• 70671-90-8 1,1-dibromo-2,2-bis(4-methylphenyl)cyclopropane 
• 611-97-2 bis(p-methylphenyl)-methanone 
• 40938-15-6 4,4’-(propa-1,2-diene-1,1-diyl)bis(methylbenzene) 
• 7789-89-1 1,1,1-trichloropropane 
• 108-88-3 toluene 
• 105-37-3 Ethyl propionate 
• 82357-51-5 4,4'-(2-bromoprop-1-ene-1,1-diyl)bis(methylbenzene) 
• 56860-31-2 1,1-bis(p-methylphenyl)cyclopropane 
• 768295-67-6 1,1-di-p-tolylpropan-1-ol 
• 74-85-1 ethene 
• 1143-91-5 bis(4-methylphenyl)diazomethane 
• 925-90-6 ethylmagnesium bromide 
• 22125-38-8 1,1-dichloro-2,2-bis(p-methylphenyl)cyclopropane 
• 2919-20-2 1,1-di(p-tolyl)ethylene 

Downstream Products

• 82357-51-5 4,4'-(2-bromoprop-1-ene-1,1-diyl)bis(methylbenzene) 
• 94311-56-5 1-Acetoxy-1.1-di--2-nitro-propan 
• 93407-42-2 1.1-Di--2-nitro-propanol-(1) 
• 106403-95-6 2-chloro-1,1-bis(p-methylphenyl)propene 

Relevant articles and documents

Regioselective Diboron-Mediated Semireduction of Terminal Allenes

A method for the regioselective reduction of the terminal double bond of 1,1-disubstituted allenes has been developed. In the presence of a palladium catalyst, tetrahydroxydiboron and stoichiometric water, allene semireduction proceeds in high yield to afford Z-alkenes selectively.

Rhodium-katalysierte Synthese dreifach substituierter Olefine aus Ethen-Derivaten und Diazoalkanen

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ARYLCYCLOPROPANE PHOTOCHEMISTRY. SUBSTITUENT EFFECTS ON THE PHOTOCHEMICAL CONVERSION OF 1,1-DIARYLCYCLOPROPANES TO 1,1-DIARYLPROPENES AND 1-ARYLINDANES.

The rate of photochemical rearrangement of 1,1-diarylcyclopropanes to 1,1-diarylpropenes and 1-arylindanes is enhanced by electron-withdrawing groups on the aromatic rings and diminished by electron-donating groups.