126314-17-8

Basic information

• Product Name: 1-(4-chlorophenyl)-4-phenylbutan-1-ol
• Synonyms: 1-(4-chlorophenyl)-4-phenylbutan-1-ol
• CAS NO: 126314-17-8
• Molecular Weight: 260.763
• Mol File: 126314-17-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-(4-chlorophenyl)-4-phenylbutan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-chlorophenyl)-4-phenylbutan-1-ol(126314-17-8)
• EPA Substance Registry System: 1-(4-chlorophenyl)-4-phenylbutan-1-ol(126314-17-8)

Safety Data

• Hazardous Substances Data: 126314-17-8(Hazardous Substances Data)

Upstream product

• 1462-75-5 3-phenylpropylmagnesium bromide 
• 104-88-1 4-chlorobenzaldehyde 
• 142389-19-3 tris(3-phenylpropyl)borane 

Downstream Products

• 126314-19-0 4-phenyl-1-(p-chlorophenyl)-4-butanone 
• 37562-71-3 4-phenyl-1-(p-chlorophenyl)-2-butanone 
• 37985-07-2 (E)-1-chloro-4-(4-phenylbut-1-en-1-yl)benzene 
• 126314-18-9 4-phenyl-1-(p-chlorophenyl)-1-butanone 
• 40845-94-1 1-(4-chlorophenyl)-1,2,3,4-tetrahydronaphthalene 

Relevant articles and documents

Enantioselective alkylation of aldehydes using functionalized alkylboron reagents catalyzed by a chiral titanium complex

A practical method is developed for the synthesis of enantioenriched functionalized secondary alcohols through catalytic enantioselective alkylation of aldehydes. Functionalized alkylboron reagents, [FG-(CH2) n]3B (FG = Br, TIPSO, PhtN, CO2iPr, and CN) prepared from terminal olefin precursors by hydroboration, undergo enantioselective addition to aldehydes in the presence of a catalytic amount (5 mol %) of 3-(3,5-diphenylphenyl)-H8-BINOL and excess titanium tetraisopropoxide to afford the corresponding functionalized alcohols in high enantioselectivities up to 99% ee.