70547-85-2

Basic information

• Product Name: 1,3,6-triphenylhexane
• Synonyms: 1,3,6-triphenylhexane
• CAS NO: 70547-85-2
• Molecular Weight: 314.47
• Mol File: 70547-85-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,3,6-triphenylhexane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,6-triphenylhexane(70547-85-2)
• EPA Substance Registry System: 1,3,6-triphenylhexane(70547-85-2)

Safety Data

• Hazardous Substances Data: 70547-85-2(Hazardous Substances Data)

Upstream product

• 106020-40-0 1,3,6-triphenyl-3-hexanol 
• 100-42-5 styrene 
• 637-59-2 1-Bromo-3-phenylpropane 
• 106020-32-0 tris(benzothieno)<3,2-b:2',3'-d:2'',3''-f>oxepin 
• 103-63-9 1-phenyl-2-bromoethane 
• 1083-30-3 dihydrochalcone 
• 614-47-1 1,3-diphenyl-propen-3-one 

Relevant articles and documents

Comparison of the regiochemical behavior of zirconium and hafnium in the polyinsertion of styrenes

The hafnocene-based catalyst ethylenebis(1-indenyl)hafnium dichloride/methylalumoxane, as well as its zirconium analogue, is able to oligomerize styrene, p-methylstyrene, and p-tert-butylstyrene in the presence of hydrogen to produce hydrooligomers. The c

CYCLOCONDENSATION OF 3(2H)-BENZOTHIOPHENONE AND OXIDATION PRODUCTS OBTAINED DURING THESE REACTIONS

The cyclocondensation of 3(2H)-benzothiophenone under acidic conditions has been studied.The symmetrical cyclotrimer tris(benzothieno)benzene was formed and under certain conditions also a rearranged cyclotrimer, tris(benzothieno)benzene.The formation of cyclotrimers was accompanied by oxidative coupling products involving the initially formed dimeric compound, 3-hydroxy-2,3-bibenzothienyl.During several of these reactions, a novel heterocycle, tris(benzothieno)oxepin, was formed.The products were studied by mass spectrometry and fragmentation pathways were determined by a linked scanning technique.