86088-39-3

Basic information

• Product Name: Oxirane, (4-phenylbutyl)-
• CAS NO: 86088-39-3
• Molecular Formula: C12H16O
• Molecular Weight: 176.258
• Mol File: 86088-39-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Oxirane, (4-phenylbutyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxirane, (4-phenylbutyl)-(86088-39-3)
• EPA Substance Registry System: Oxirane, (4-phenylbutyl)-(86088-39-3)

Safety Data

• Hazardous Substances Data: 86088-39-3(Hazardous Substances Data)

Upstream product

• 87100-28-5 pinacol benzylboronate 
• 21746-87-2 5-bromo-1,2-epoxypentane 
• 36884-28-3 5-phenyl-1-pentanal 
• 10521-91-2 5-phenylpentan-1-ol 
• 1588-44-9 6-phenyl-1-hexene 

Downstream Products

• 14171-89-2 1-phenyl-5-hexanone 
• 859770-94-8 1-dimethylamino-6-phenyl-hexan-2-ol 
• 86088-41-7 1,2-benzocyclohepten-3-ylmethanol 
• 68480-12-6 2-(1,2,3,4-tetrahydronaphthalen-1-yl)ethanol 
• 89789-89-9 2-Hydroxy-5-[2-(2-hydroxy-6-phenyl-hexylamino)-ethoxy]-benzamide 
• 821785-90-4 (R)-8-phenyloct-1-en-4-ol 
• 397871-03-3 (6R)-6-[(1E,4R,6R)-4,6-dihydroxy-10-phenyldec-1-en-1-yl]-5,6-dihydro-2H-pyran-2-one 
• 934473-37-7 tert-butyl-{4-[2,2-dimethyl-6-(4-phenyl-butyl)-[1,3]dioxan-4-yl]-1-[2-(4-methoxy-benzyloxy)-ethyl]-but-2-enyloxy}-dimethyl-silane 
• 934473-35-5 9-(tert-butyl-dimethyl-silanyloxy)-1-(4-methoxy-benzyloxy)-13-phenyl-tridec-4-yne-3,7-diol 
• 934473-25-3 5-(tert-butyl-dimethyl-silanyloxy)-8-[2,2-dimethyl-6-(4-phenyl-butyl)-[1,3]dioxan-4-yl]-octa-2,6-dienoic acid methyl ester 
• 934473-36-6 6-[2,2-dimethyl-6-(4-phenyl-butyl)-[1,3]dioxan-4-yl]-1-(4-methoxy-benzyloxy)-hex-4-yn-3-ol 
• 934473-26-4 1-(4-methoxy-benzyloxy)-13-phenyl-tridec-4-yne-3,7,9-triol 
• 934473-30-0 6-[2,2-dimethyl-6-(4-phenyl-butyl)-[1,3]dioxan-4-yl]-1-(4-methoxy-benzyloxy)-hex-4-en-3-ol 
• 934473-31-1 3-(tert-butyl-dimethyl-silanyloxy)-6-[2,2-dimethyl-6-(4-phenyl-butyl)-[1,3]dioxan-4-yl]-hex-4-en-1-ol 

Relevant articles and documents

Transition Metal-Free sp3?sp3 Carbon-Carbon Coupling between Benzylboronic Esters and Alkyl Bromides

A transition metal-free coupling reaction of benzylboronic esters and alkyl halides has been developed. Both alkyl bromides and alkyl iodides were found to be competent substrates with the nucleophilic boronate intermediate generated from the combination of benzylboronic ester and an alkyllithium. Good chemoselectivity was observed for the reaction with the alkyl bromide in substrates with a second electrophile present. Both secondary and tertiary benzylboronic esters were effective nucleophiles in the reaction with primary alkyl halides. Mechanistic observations are consistent with a radical mechanism.