ChemicalBook--->CAS DataBase List--->6705-49-3

6705-49-3

6705-49-3 Structure

6705-49-3 Structure
IdentificationBack Directory
[Name]

7-OXABICYCLO[4.1.0]HEPTAN-2-ONE
[CAS]

6705-49-3
[Synonyms]

2,3-Epoxycyclohexanone
2,3-Epoxy-1-cyclohexanone
2,3-Epoxycyclohexan-1-one
Cyclohexanone, 2,3-epoxy-
7-OXABICYCLO[4.1.0]HEPTAN-2-ONE
7-oxabicyclo[4.1.0]heptan-5-one
7-Oxabicyclo[4.1.0]heptan-2-one 98%
(1R,6R)-7-oxabicyclo[4.1.0]heptan-5-one
7-Oxabicyclo[4.1.0]heptan-2-one(6CI,7CI,8CI,9CI)
7-Oxabicyclo[4.1.0]heptan-2-one (6CI, 7CI, 8CI, 9CI, ACI)
[EINECS(EC#)]

229-751-4
[Molecular Formula]

C6H8O2
[MDL Number]

MFCD00192371
[MOL File]

6705-49-3.mol
[Molecular Weight]

112.13
Chemical PropertiesBack Directory
[Boiling point ]

76-78 °C15 mm Hg(lit.)
[density ]

1.13 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.474(lit.)
[Fp ]

205 °F
[storage temp. ]

2-8°C
Safety DataBack Directory
[WGK Germany ]

3
[HS Code ]

2932990090
Hazard InformationBack Directory
[Uses]

7-Oxabicyclo[4.1.0]heptan-2-one was employed as substrate to investigate the substrate specificity of purified recombinant NADPH-dependent 3-quinuclidinone reductases from Microbacterium luteolum JCM 9174 for the reductive reaction of ketones.
[Synthesis Reference(s)]

The Journal of Organic Chemistry, 48, p. 4931, 1983 DOI: 10.1021/jo00173a029
[General Description]

7-Oxabicyclo[4.1.0]heptan-2-one is one of the products formed during oxidation of cyclohexene by dendritic complexes. It has been reported as anticapsin analog.
Spectrum DetailBack Directory
[Spectrum Detail]

7-OXABICYCLO[4.1.0]HEPTAN-2-ONE(6705-49-3)IR
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