114920-74-0

Basic information

• Product Name: 1,1,4,4-tetrakis(4-methylphenyl)buta-1,2,3-triene
• Synonyms: 1,1,4,4-tetrakis(4-methylphenyl)buta-1,2,3-triene
• CAS NO: 114920-74-0
• Molecular Weight: 412.574
• Mol File: 114920-74-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,1,4,4-tetrakis(4-methylphenyl)buta-1,2,3-triene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,4,4-tetrakis(4-methylphenyl)buta-1,2,3-triene(114920-74-0)
• EPA Substance Registry System: 1,1,4,4-tetrakis(4-methylphenyl)buta-1,2,3-triene(114920-74-0)

Safety Data

• Hazardous Substances Data: 114920-74-0(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 123-51-3 i-Amyl alcohol 
• 824413-79-8 2,3-dichloro-1,1,4,4-tetra-p-tolyl-but-2-ene 
• 141-52-6 sodium ethanolate 
• 855232-28-9 1,1,4,4-tetrakis(4-methylphenyl)but-2-yne-1,4-diol 
• 93318-88-8 1,1-bis(4-methylphenyl)-2-propyn-1-ol 
• 611-97-2 bis(p-methylphenyl)-methanone 
• 28437-54-9 1,1'-(3-methoxyprop-1-yne-3,3-diyl)bis(4-methylbenzene) 
• 1626481-27-3 4-methoxy-1,1,4,4-tetrakis(4-methylphenyl)but-2-yn-1-ol 
• 60-29-7 diethyl ether 

Downstream Products

• 33861-11-9 1,1,4,4-Tetrakis(4-methylphenyl)-1,3-butadiene 
• 118091-30-8 2-(2,2-Di-p-tolyl-vinyl)-6-methyl-3-p-tolyl-benzo[b]selenophene 
• 118091-24-0 6,7-Bis-di-p-tolylmethylene-[1,2,3,4,5]pentathiepane 
• 118091-27-3 3,4,6,7-Tetrakis-di-p-tolylmethylene-[1,2,5]triselenepane 
• 611-97-2 bis(p-methylphenyl)-methanone 

Relevant articles and documents

Mechanosynthesis of Odd-Numbered Tetraaryl[n]cumulenes

A mechanochemical synthesis of one-dimensional carbon allotrope carbyne model compounds, namely tetraaryl[n]cumulenes (n=3, 5) was realized. Central for the mechanosynthesis of the cumulenic carbon nanostructures were the development of a mechanochemical Favorskii alkynylation-type reaction and the implementation of a solvent-free, acid-free reductive elimination with tin(II) chloride by ball milling.

Synthesis of cyano-substituted diaryltetracenes from tetraaryl[3]cumulenes

A versatile, two-step synthesis of highly substituted, cyano-functionalized diaryltetracenes has been developed, starting from easily accessible tetraaryl[3]cumulenes. This unprecedented transformation is initiated by [2+2] cycloaddition of tetracyanoethy