31024-89-2

Basic information

• Product Name: α,α'-diphenyl-1,4-benzenedimethanol
• CAS NO: 31024-89-2
• Molecular Weight: 290.362
• Mol File: 31024-89-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: α,α'-diphenyl-1,4-benzenedimethanol(CAS DataBase Reference)
• NIST Chemistry Reference: α,α'-diphenyl-1,4-benzenedimethanol(31024-89-2)
• EPA Substance Registry System: α,α'-diphenyl-1,4-benzenedimethanol(31024-89-2)

Safety Data

• Hazardous Substances Data: 31024-89-2(Hazardous Substances Data)

Upstream product

• 3016-97-5 1,4-dibenzoylbenzene 
• 100-52-7 benzaldehyde 
• 64-17-5 ethanol 
• 793-23-7 1,4-dibenzylbenzene 
• 623-27-8 terephthalaldehyde, 
• 98-80-6 phenylboronic acid 
• 100-58-3 phenylmagnesium bromide 
• 591-51-5 phenyllithium 
• 60-29-7 diethyl ether 
• 106-42-3 para-xylene 
• 1592-31-0 1,4-bis(dibromomethyl)benzene 

Downstream Products

• 6606-72-0 meso-1.4-bis-(α-chloro-benzyl)-benzene 
• 6606-72-0 racem.-1.4-bis-(α-chloro-benzyl)-benzene 
• 3016-97-5 1,4-dibenzoylbenzene 
• 6606-72-0 1,4-bis(α-chlorobenzyl)benzene 
• 917-23-7 5,15,10,20-tetraphenylporphyrin 
• 130870-28-9 C₂₄H₂₂S₄ 
• 1186025-57-9 1,4-bis(phenyl(2-pyrrolyl)methyl)benzene 
• 31020-20-9 (4-(hydroxy(phenyl)methyl)phenyl)(phenyl)methanone 
• 95560-57-9 α,α'-diphenyl-1,4-benzenedimethanol diacetate 
• 66837-44-3 1,4-bis(α-bromobenzyl)benzene 

Relevant articles and documents

Selective mono addition of aryllithiums to dialdehydes by micromixing

Micromixing enables highly selective mono addition of aryllithiums to dialdehydes. Because the unchanged formyl group in the products can be used for further transformations, the present approach serves as a powerful method for protecting-group-free synthesis.

An unusual chemoselective oxidation strategy by an unprecedented exploration of an electrophilic center of DMSO: A new facet to classical DMSO oxidation

A conceptually new dimethyl sulfoxide (DMSO) based oxidation process without the use of any activator has been demonstrated for the oxidation of active methylenes and benzhydrols. The developed protocol utilizes the electrophilic center of DMSO for oxidation, which was unexplored before. Mechanistic investigation has confirmed that the source of oxygen is DMSO.

Steric control in the synthesis of p-benziporphyrins. formation of a doubly n-confused benzihexaphyrin macrocycle

The use of 1,4-phenylene-containing tripyrrane analogs provides a general route to expanded p-benziporphyrins. The course of macrocyclization shows a striking dependence on the steric bulk of meso substituents.