137438-51-8

Basic information

• Product Name: Benzene, [[(1-phenyl-3-butenyl)oxy]methyl]-
• CAS NO: 137438-51-8
• Molecular Formula: C17H18O
• Molecular Weight: 238.329
• Mol File: 137438-51-8.mol
• Article Data: 21

Chemical Properties

• CAS DataBase Reference: Benzene, [[(1-phenyl-3-butenyl)oxy]methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [[(1-phenyl-3-butenyl)oxy]methyl]-(137438-51-8)
• EPA Substance Registry System: Benzene, [[(1-phenyl-3-butenyl)oxy]methyl]-(137438-51-8)

Safety Data

• Hazardous Substances Data: 137438-51-8(Hazardous Substances Data)

Upstream product

• 14642-79-6 benzyloxy-trimethylsilane 
• 100-52-7 benzaldehyde 
• 762-72-1 allyl-trimethyl-silane 
• 100-51-6 benzyl alcohol 
• 5784-65-6 benzaldehyde dibenzyl acetal 
• 72824-04-5 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 80735-94-0 1-Phenyl-3-buten-1-ol 
• 936-51-6 2-phenyl-1,3-dioxolane 
• 100-39-0 benzyl bromide 

Downstream Products

• 405114-21-8 2-[2-(benzyloxy)-2-phenylethyl]-1-(tert-butoxycarbonyl)-1,2,3,6-tetrahydropyridine 
• 1537222-98-2 4-(benzyloxy)-4-phenylbutanal 
• 1229611-16-8 (E)-(1-(benzyloxy)but-2-en-1-yl)benzene 
• 1219706-14-5 4-(benzyloxy)-4-phenylbutane-1,2-diyl diacetate 
• 176444-41-0 5-phenyltetrahydrofuran-3-yl acetate 
• 140854-79-1 (anti)-1-(benzyloxy)-4,4-dimethyl-1-phenyl-5-hexen-3-ol 
• 140854-78-0 (syn)-1-(benzyloxy)-4,4-dimethyl-1-phenyl-5-hexen-3-ol 
• 140854-61-1 1-(benzyloxy)-3,3--1-phenylpropane 
• 132816-14-9 1-(benzyloxy)-3-<(3-methyl-2-butenyl)oxy>-1-phenyl-3-(phenylthio)propane 
• 112476-31-0 1-(1-benzyloxybutyl)benzene 
• 3145-76-4 (2-methylcyclopropyl)benzene 
• 824-90-8 1-phenylbut-1-ene 

Relevant articles and documents

Anti-Markovnikov Hydrofunctionalization of Alkenes: Use of a Benzyl Group as a Traceless Redox-Active Hydrogen Donor

A protocol for the anti-Markovnikov hydrofunctionalization of alkenes has been developed by the use of a benzyl group as a traceless redox-active hydrogen donor. Under copper catalysis and in the presence of CF3- or N3-containing hyp

Iron-catalysed, general and operationally simple formal hydrogenation using Fe(OTf)3 and NaBH4

An operationally simple and environmentally benign formal hydrogenation protocol has been developed using highly abundant iron(iii) salts and an inexpensive, bench stable, stoichiometric reductant, NaBH4, in ethanol, under ambient conditions. This reaction has been applied to the reduction of terminal alkenes (22 examples, up to 95% yield) and nitro-groups (26 examples, up to 95% yield). Deuterium labelling studies indicate that this reaction proceeds via an ionic rather than radical mechanism.

Cesium salt of tungstosilicic acid fabricated by nano-casting strategy: An efficient catalyst for the three-component Hosomi-Sakurai reaction

We have used SBA-15 silicas as hard templates for the nano-fabrication of Cs1.8H2.2SiW12O40 (CsHSiW) salt nanocrystal. The elimination by HF (or NaOH 90 °C) in the silica matrix from the composites occurred by a