93222-37-8

Basic information

• Product Name: 4-phenylpent-4-en-1-ol
• Synonyms: 4-phenylpent-4-en-1-ol
• CAS NO: 93222-37-8
• Molecular Weight: 162.232
• Mol File: 93222-37-8.mol
• Article Data: 24

Chemical Properties

• CAS DataBase Reference: 4-phenylpent-4-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenylpent-4-en-1-ol(93222-37-8)
• EPA Substance Registry System: 4-phenylpent-4-en-1-ol(93222-37-8)

Safety Data

• Hazardous Substances Data: 93222-37-8(Hazardous Substances Data)

Upstream product

• 5390-04-5 pent-1-yn-5-ol 
• 98-80-6 phenylboronic acid 
• 78687-92-0 ethyl 4-phenyl-4-pentenoate 
• 25333-24-8 3-benzoylpropionic acid methyl ester 
• 1392108-22-3 O-(4-phenylpent-4-enyl)-N-benzoyl-N-phenylhydroxylamine 
• 6089-09-4 4-pentynoic acid 
• 194805-62-4 methyl-4-bromo-pent-4-enoate 
• 93863-05-9 4-phenylpent-4-enoic acid methyl ester 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 2051-95-8 succinylbenzene 
• 182194-88-3 4-phenylpent-4-en-1-yl 4-methylbenzenesulfonate 
• 5747-06-8 4-phenylpent-4-enoic acid 
• 195213-60-6 4-(4-chlorophenyl)-3-(4-phenylpent-4-enyloxy)-1,3-thiazole-2(3H)-thione 
• 39755-03-8 4-hydroxy-1-phenyl-butan-1-one 

Downstream Products

• 174905-67-0 2,4,4-Trimethyl-5-phenyl-1-thioxo-1,2,4,6,7,8-hexahydro-pyrido[1,2-c]pyrimidin-3-one 
• 1262757-71-0 4-methyl-N-(4-phenylpent-4-en-1-yl)benzenesulfonamide 
• 1304754-56-0 (R)-2-(bromomethyl)-1-(4-nitrophenylsulfonyl)-2-phenylpyrrolidine 
• 1304756-05-5 (S)-2-(bromomethyl)-1-(4-nitrophenylsulfonyl)-2-phenylpyrrolidine 
• 1304754-59-3 (R)-2-(bromomethyl)-1-(3-nitrophenylsulfonyl)-2-phenylpyrrolidine 
• 1304754-62-8 (R)-2-(bromomethyl)-1-(2-nitrophenylsulfonyl)-2-phenylpyrrolidine 
• 1304754-74-2 (R)-2-(bromomethyl)-1-(3,5-difluorophenylsulfonyl)-2-phenylpyrrolidine 
• 1304755-24-5 (R)-5-phenyl-1-azabicyclo[3.1.0]hexane 
• 1304755-28-9 (R)-5-(bromomethyl)-1-(4-nitrophenylsulfonyl)-5-phenylpyrrolidin-2-one 
• 1304753-57-8 4-nitro-N-(4-phenylpent-4-en-1-yl)benzenesulfonamide 
• 1304753-61-4 3-nitro-N-(4-phenyl-4-pentenyl)benzenesulfonamide 
• 1304753-65-8 2-nitro-N-(4-phenyl-4-pentenyl)benzenesulfonamide 
• 1304753-80-7 N-(4-phenyl-4-pentenyl)benzenesulfonamide 
• 1304753-86-3 3,5-difluoro-N-(4-phenyl-4-pentenyl)benzenesulfonamide 

Relevant articles and documents

Bis(trifluoromethanesulfonimide) (BSI): Acidity and application to hydrofunctionalization as a Br?nsted acid catalyst

A binaphthyl derivative, bearing bis(trifluoromethanesulfonimide) (BSI) moiety, was developed as a novel Br?nsted acid. Computational prediction of the pKa value of BSI indicated its classification as a strong Br?nsted acid. BSI catalyzed the h

Copper-Catalyzed Modular Amino Oxygenation of Alkenes: Access to Diverse 1,2-Amino Oxygen-Containing Skeletons

Copper-catalyzed alkene amino oxygenation reactions using O-acylhydroxylamines have been achieved for a rapid and modular access to diverse 1,2-amino oxygen-containing molecules. This transformation is applicable to the use of alcohols, carbonyls, oximes, and thio-carboxylic acids as nucleophiles on both terminal and internal alkenes. Mild reaction conditions tolerate a wide range of functional groups, including ether, ester, amide, carbamate, and halide. The reaction protocol allows for starting with free amines as the precursor of O-benzoylhydroxylamines to eliminate their isolation and purification, contributing to broader synthetic utilities. Mechanistic investigations reveal the amino oxygenation reactions may involve distinct pathways, depending on different oxygen nucleophiles.

Double Functionalization of Styrenes by Cu-Mediated Assisted Tandem Catalysis

The double functionalization of styrenes through Cu-mediated assisted tandem catalysis was developed. The reaction was initiated by Cu-catalyzed aziridination and the subsequent nucleophilic ring-opening, which was triggered by the addition of (NH4)2S2O8 as an oxidant of Cu-catalyst to form a variety of C–C and C–X bonds. The expansion to three contiguous catalytic cycles led to the synthesis of functionalized indolines by one-pot operation.