| Identification | Back 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 Properties | Back 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 | [form ]
liquid |
| Hazard Information | Back 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. |
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