1192167-43-3

Basic information

• Product Name: 1,1-diphenyl-3-p-fluorophenylpropargyl alcohol
• Synonyms: 1,1-diphenyl-3-p-fluorophenylpropargyl alcohol
• CAS NO: 1192167-43-3
• Molecular Weight: 302.348
• Mol File: 1192167-43-3.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 1,1-diphenyl-3-p-fluorophenylpropargyl alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-diphenyl-3-p-fluorophenylpropargyl alcohol(1192167-43-3)
• EPA Substance Registry System: 1,1-diphenyl-3-p-fluorophenylpropargyl alcohol(1192167-43-3)

Safety Data

• Hazardous Substances Data: 1192167-43-3(Hazardous Substances Data)

Upstream product

• 766-98-3 1-ethynyl-4-fluorobenzene 
• 91-01-0 1,1-Diphenylmethanol 
• 119-61-9 benzophenone 

Downstream Products

• 1192167-54-6 3-(4-fluorophenyl)-5,7-dimethyl-1,1-diphenyl-1H-inden-6-ol 
• 1242072-92-9 4-benzhydryl-5-(4-fluorophenyl)-2-methylthiazole 
• 1263098-40-3 4-benzhydryl-5-(4-fluorophenyl)-2-phenyloxazole 
• 1266570-24-4 diethyl 1-(4-fluorophenyl)-3,3-diphenylpropa-1,2-dienyl(p-tolyl)phosphoramidate 
• 1341179-10-9 diethyl 1-ethyl-4-(4-fluorophenyl)-7-methyl-6,6-diphenyl-6,7-dihydro-1H-azepine-2,3-dicarboxylate 
• 1415035-06-1 3-(4-fluorophenyl)-5,5-diphenyl-2-tosyl-2,5-dihydroisoxazole 
• 1373883-78-3 1-(4-fluorophenyl)-4-methyl-3,3-diphenyl-3,4-dihydrocyclopenta[b]indole 
• 1373883-97-6 3-(3-(4-fluorophenyl)-1,1-diphenylprop-2-yn-1-yl)-1-methyl-1H-indole 
• 1373884-07-1 3-(4-fluorophenyl)-2-iodo-4-methyl-1,1-diphenyl-1,4-dihydrocyclopenta[b]indole 
• 1620975-18-9 N-(4-fluorophenyl)-3,3-diphenylacrylamide 

Relevant articles and documents

Lewis Acid Catalyzed Cyclization of Propargylic Alcohols with 2-Vinylphenol

An unprecedented Lewis acid catalyzed, protection-free, and high-efficiency synthesis of valuable 3,4-dihydro-2H-2,4-methanochromans via cycloaddition of propargylic alkynols with 2-vinylphenol is described. This cycloaddition protocol, which tolerates a

Lewis-Acid-Catalyzed Tandem Cyclization by Ring Expansion of Tertiary Cycloalkanols with Propargyl Alcohols

A new method for the efficient synthesis of hexahydro-1H-fluorene and octahydrobenzo[a]azulene derivatives through a ring-expansion strategy is reported. With an appropriate combination of thulium(III) trifluoromethanesulfonate and 13X molecular sieves, a range of unsaturated polycyclic compounds were obtained in good yields. Mechanism studies reveal that the reaction is more likely to undergo Meyer–Schuster rearrangement, ring expansion, and Friedel–Crafts-type pathways, which provide a conceptually different strategy for the ring opening of tertiary cycloalkanols.

Br?nsted Acid-Mediated Formal [3+3] Annulation Between Propargylic Alcohols and 1,3-Diketones

A Br?nsted acid-mediated formal [3+3] cascade annulation of propargylic alcohols with 1,3-diketones proceeds through a sequential Meyer?Schuster rearrangement/1,2-addition. This protocol, which has a wide scope and is conducted under an ambient atmosphere