105337-73-3

Basic information

• Product Name: (E)-5-o-tolylpent-4-en-1-ol
• CAS NO: 105337-73-3
• Molecular Weight: 176.258
• Mol File: 105337-73-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (E)-5-o-tolylpent-4-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-5-o-tolylpent-4-en-1-ol(105337-73-3)
• EPA Substance Registry System: (E)-5-o-tolylpent-4-en-1-ol(105337-73-3)

Safety Data

• Hazardous Substances Data: 105337-73-3(Hazardous Substances Data)

Upstream product

• 939400-91-6 5-o-tolylpent-4-enoic acid ethyl ester 
• 110-87-2 3,4-dihydro-2H-pyran 
• 195062-59-0 2-methylphenylboronic acid pinacol ester 
• 87436-78-0 (4-hydroxybutyl)-triphenylphosphonium bromide 
• 529-20-4 2-methylphenyl aldehyde 
• 445477-03-2 5-(2-methylphenyl)-4-pentenoic acid 
• 5631-95-8 2,3-dichlorotetrahydro-2H-pyran 
• 95-46-5 2-methylphenyl bromide 

Downstream Products

• 1380523-52-3 (E)-5-o-tolylpent-4-enyl methanesulfonate 
• 1380523-12-5 (E)-dimethyl 2-(5-o-tolylpent-4-enyl)malonate 
• 1426692-66-1 3-chloro-2-o-tolyltetrahydro-2H-pyran 
• 15382-80-6 1-o-Tolyl-5-<4-amino-2-methoxy-phenoxy>-pentan 
• 109808-88-0 1-o-Tolyl-5-(4-nitro-2-methoxy-phenoxy)-pentan 
• 105474-56-4 O-(5-bromopentyl)-toluene 
• 107055-19-6 5-o-Tolyl-pentanol-⁽¹⁾ 

Relevant articles and documents

Nickel-catalyzed ring-opening cross-coupling of cyclic alkenyl ethers with arylboronic esters via carbon-oxygen bond cleavage

We have developed a nickel-catalyzed cross-coupling reaction of cyclic alkenyl ethers with arylboronic esters that leads to the formation of unsaturated alcohols via ring-opening by the cleavage of a C(sp2)-O bond. The use of 1,3-dicyclohexylimidazol-2-ylidene as the ligand is essential to promote this cross-coupling process.

Manganese(III) acetate mediated oxidative radical cyclizations. Toward vicinal all-carbon quaternary stereocenters

Manganese(III) acetate mediated oxidative radical cyclizations have been used to synthesize a range of densely functionalized and sterically congested cyclopentane-lactones. A number of the resulting lactones contain vicinal all-carbon quaternary stereocenters adjacent to a tertiary benzylic stereocenter and are formed with high levels of stereocontrol.