1065544-48-0

Basic information

• Product Name: (phenyl)[2-(thien-2-yl)phenyl]methanol
• Synonyms: (phenyl)[2-(thien-2-yl)phenyl]methanol
• CAS NO: 1065544-48-0
• Molecular Weight: 266.364
• Mol File: 1065544-48-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (phenyl)[2-(thien-2-yl)phenyl]methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (phenyl)[2-(thien-2-yl)phenyl]methanol(1065544-48-0)
• EPA Substance Registry System: (phenyl)[2-(thien-2-yl)phenyl]methanol(1065544-48-0)

Safety Data

• Hazardous Substances Data: 1065544-48-0(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 106851-53-0 2-(2’-bromophenyl)thiophene 
• 99902-07-5 2-(2-thienyl)benzaldehyde 
• 100-58-3 phenylmagnesium bromide 
• 108-86-1 bromobenzene 
• 615-36-1 2-bromoaniline 

Downstream Products

• 1065544-54-8 acetic acid (phenyl)[2-(thien-2-yl)phenyl]methyl ester 
• 1065544-75-3 8-phenyl-8H-3-thia-cyclopenta[a]indene 

Relevant articles and documents

Highly efficient synthesis of polysubstituted fluorene via iron-catalyzed intramolecular Friedel-Crafts alkylation of biaryl alcohols

An efficient and mild Fe(III)-catalyzed intramolecular Friedel-Crafts alkylation of biaryl methanol derivatives has been developed to achieve the substituted fluorene derivatives. The present reaction provides an excellent alternative to published methods

Potentially Aromatic Thiophenium Ylides. V. Reactions of Ethoxycarbonyl- (and Methoxycarbonyl)-2-(2-thienyl)phenylcarbene

In an attempt to make thiophenium ylides in which the ylide bond is part of a five-membered ring annulated to the α-side of the thiophene moiety, two alkoxycarbonyl substituted 2-(2-thienyl)phenylcarbenes have been made, with and without chlorine substituents in the remaining thiophene positions.With rhodium acetate as a catalyst the carbene without chlorines cyclized to the 3-position of the thiophene to give a fluorene analogue, whereas no cyclization was detected when the 3-position was blocked.