14503-58-3

Basic information

• Product Name: 2-Butenyl(phenyl) ether
• Synonyms: 2-Butenyl(phenyl) ether;2-Butenyloxybenzene;4-PHENOXY-2-BUTENE
• CAS NO: 14503-58-3
• Molecular Formula: C₁₀H₁₂O
• Molecular Weight: 148.2
• Mol File: 14503-58-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 98-98.5 °C(Press: 14 Torr)
• Appearance: /
• Density: 0.946±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-Butenyl(phenyl) ether(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Butenyl(phenyl) ether(14503-58-3)
• EPA Substance Registry System: 2-Butenyl(phenyl) ether(14503-58-3)

Safety Data

• Hazardous Substances Data: 14503-58-3(Hazardous Substances Data)

Upstream product

• 4784-77-4 (E/Z)-crotyl bromide 
• 67-64-1 acetone 
• 108-95-2 phenol 
• 101-84-8 diphenylether 
• 591-97-9 1-chloro-2-butene 
• 106-99-0 buta-1,3-diene 
• 14309-15-0 phenyl prenyl ether 
• 122898-55-9 1-methyl-propenyl phenyl carbonate 
• 91668-28-9 2-butenyl phenyl carbonate 
• 87280-00-0 1‐bromo‐2‐(but-3‐en‐1‐yloxy)benzene 
• 56182-34-4 o-(but-3-enyoxy)phenyl radical 

Downstream Products

• 22409-85-4 4-phenoxybutan-2-one 
• 161268-30-0 1-phenoxy-2-butanone 
• 37849-09-5 2-(but-2-enyl)-1,4-dimethylbenzene 
• 116043-56-2 1-phenoxy-3-methyl-1Z-hepten-4-ol 
• 934-10-1 3-phenylbut-1-ene 
• 1560-06-1 1-phenyl-2-butene 
• 61904-01-6 4-phenoxy-2-butanol 
• 4317-72-0 1-phenoxy-2-butanol 
• 18272-63-4 2-(but-3-en-2-yl)phenol 
• 64-18-6 formic acid 
• 64-19-7 acetic acid 
• 1126-79-0 n-butyl phenyl ether 
• 18448-88-9 2-crotylphenol 
• 108-95-2 phenol 

Relevant articles and documents

METHOD FOR PRODUCING ARENE COMPOUNDS AND ARENE COMPOUNDS PRODUCED BY THE SAME

Provided is a method for producing (alkyl)arene compounds represented by Formulae 3-1, 3-2, and 3-3 by the Friedel-Crafts alkylation reaction of alkyl halide compounds and arene compounds using organic phosphine compounds as a catalyst.

Regioselective iron-catalyzed decarboxylative allylic etherification

[Chemical Equation Presented] An anionic iron complex catalyzes the decarboxylative allylation of phenols to form allylic ethers in high yield. The allylation is regioselective rather than regiospecific. This suggests that the allylation proceeds through π-allyl iron intermediates in contrast to related allylations of carbon nucleophiles that have been proposed to proceed via π-allyl complexes. Ultimately, iron catalysts have the potential to replace more expensive palladium catalysts that are typically utilized for decarboxylative couplings.