5651-62-7

Basic information

• Product Name: 2-Benzoxepin-1(3H)-one, 4,5-dihydro-
• CAS NO: 5651-62-7
• Molecular Formula: C10H10O2
• Molecular Weight: 162.188
• Mol File: 5651-62-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Benzoxepin-1(3H)-one, 4,5-dihydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Benzoxepin-1(3H)-one, 4,5-dihydro-(5651-62-7)
• EPA Substance Registry System: 2-Benzoxepin-1(3H)-one, 4,5-dihydro-(5651-62-7)

Safety Data

• Hazardous Substances Data: 5651-62-7(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 32552-21-9 2-(3-hydroxypropane)benzoic acid 
• 136863-23-5 3-[2-(hydroxymethyl)phenyl]propan-1-ol 
• 26930-28-9 2-(3-bromo-propoxy)-benzoic acid methyl ester 
• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 

Downstream Products

• 951388-19-5 N-[2-(3-chloro-4-methoxyphenyl)ethyl]-2-(3-hydroxypropyl)benzamide 
• 914081-50-8 2-(3-hydroxypropyl)-N-[2-(1H-indol-3-yl)ethyl]benzamide 
• 69805-03-4 2-(3-chloro-propyl)-benzoic acid 

Relevant articles and documents

Synthesis and antifungal activity of 7-methyl-7-hydroxy-2,3-benzo[c]octa-1, 6-olide

The racemic 7-methyl-7-hydroxy-2,3-benzo[c]octa-1,6-olide, the analog of natural product (6R)-3,7-dimethyl-7-hydroxy-2-octen-1,6-olide, was totally synthesized using easily available (E)-2-(2-carboxyvinyl)benzoic acid as a raw material in nine-step reacti

Radical isomerization via intramolecular ipso substitution of aryl ethers: Aryl translocation from oxygen to carbon

Bromopropyl aryl ethers an converted to 3-arylpropanols under standard radical generating conditions in the presence of tributylstannane and AIBN. This rearrangement involves intramolecular ipso attack of the alkyl radicals which generates spiro cyclohexadienyl radical intermediates.