50599-57-0

Basic information

• Product Name: Furan, 2,5-dihydro-2,2,5,5-tetraphenyl-
• CAS NO: 50599-57-0
• Molecular Formula: C28H22O
• Molecular Weight: 374.482
• Mol File: 50599-57-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Furan, 2,5-dihydro-2,2,5,5-tetraphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Furan, 2,5-dihydro-2,2,5,5-tetraphenyl-(50599-57-0)
• EPA Substance Registry System: Furan, 2,5-dihydro-2,2,5,5-tetraphenyl-(50599-57-0)

Safety Data

• Hazardous Substances Data: 50599-57-0(Hazardous Substances Data)

Upstream product

• 84072-33-3 cis-1,1,4,4-tetraphenyl-2-butene-1,4-diol 
• 1483-74-5 1,1,4,4-tetraphenyl-2-butyne-1,4-diol 
• 591-51-5 phenyllithium 
• 2639-43-2 1,1,4,4-tetraphenyl-but-2-ene-1,4-diol 
• 127-09-3 sodium acetate 
• 108-24-7 acetic anhydride 
• 67-66-3 chloroform 
• 7726-95-6 bromine 
• 50599-58-1 cis-endo-5,6-bis(hydroxydiphenylmethyl)bicyclo<2.2.1>hept-2-ene 
• 624-48-6 dimethyl cis-but-2-ene-1,4-dioate 
• 60-29-7 diethyl ether 
• 141-05-9 Diethyl maleate 

Downstream Products

• 1483-64-3 1,1,4,4-tetraphenyl-butane 
• 857821-41-1 3,4-dichloro-2,2,5,5-tetraphenyl-tetrahydro-furan 
• 119-61-9 benzophenone 

Relevant articles and documents

The Pyrolyses of 1,1,4,4-Tetraphenyl-1,4-butanediol and 1,1,4,4-Tetraphenyl-2-butene-1,4-diol Derivatives. Decomposition Reactions to Form Olefins via the Elimination of Two Mole Equivalents of the Hydroxydiphenylmethyl Radical

The pyrolysis of 1,1,2,4,4-pentaphenyl-1,4-butandiol, trans-1,2-bis(hydroxydiphenylmethyl)hexane, trans-1,2-bis(hydroxydiphenylmethyl)indan, and cis-endo- and trans-1,2-bis(hydroxydiphenylmethyl)bicycloheptane gave styrene, cyclohexene, indene, and norbornene respectively, accompanied by benzophenone and benzhydrol.The pyrolysis of trans-1,2-bis(hydroxydiphenylmethyl)spironona-4,6,8-triene afforded indene via rearrangement to form trans-1,2-bis(hydroxydiphenylmethyl)indan.The pyrolysis of cis-1,1,4,4-tetraphenyl-2-butene-1,4-diol afforded 2,2,5,5-tetraphenyl-2,5-dihydrofuran.On the other hand, trans-1,1,4,4-tetraphenyl-2- butene-1,4-diol afforded 1,2,4,4-tetraphenyl-3-buten-1-one.The mechanisms of these decomposition reactions are discussed.