| Identification | Back Directory | [Name]
(+/-)-cis-Bicyclo[3.2.0]hept-2-en-6-one | [CAS]
13173-09-6 | [Synonyms]
Bicyclohepten
BICYCLO[3.2.0]HEPT-2-EN-6-ONE
bicyclo[3.2.0]hept-3-en-7-one
Bicyclo(3.2.0)hept-2-en-6-one,96%
Bicyclo3.2.0ühept-2-en-6-one, 97%
(+/-)-cis-Bicyclo[3.2.0]hept-2-en-6-one
Bicyclo[3.2.0]hept-2-en-6-one bisulphite adduct
(+/-)-cis-Bicyclo[3.2.0]hept-2-en-6-one >=98.0%
low price (+/-)-cis-Bicyclo[3.2.0]hept-2-en-6-one
(±)-cis-Bicyclo[3.2.0]hept-2-en-6-one | [Molecular Formula]
C7H8O | [MDL Number]
MFCD00066201 | [MOL File]
13173-09-6.mol | [Molecular Weight]
108.14 |
| Chemical Properties | Back Directory | [Boiling point ]
158-160 °C(lit.)
| [density ]
1.025 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.4820(lit.)
| [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [Sensitive ]
Air Sensitive |
| Hazard Information | Back Directory | [Uses]
Bicyclo[3.2.0]hept-2-en-6-one is widely utilized to study enantioselective Baeyer-Villiger oxidation of (±)-cis-bicyclo(3.2.0)hept-2-en-6-one. It is used in the synthesis of a series of chalcone derivatives by reacting with arylaldehydes. It is also used to analyze the extremophile enzymes (monooxygenase and hydrolases) in microorganisms which are isolated from a deep-water petroleum reservoir and at high temperatures using fluorogenic assays and multibioreactions. | [General Description]
(±)-cis-bicyclo(3.2.0)hept-2-en-6-one undergoes preparative scale Baeyer–Villiger biooxidation at high concentration using recombinant Escherichia coli biocatalyst and adsorbent resin (in situ substrate feeding and product removal). |
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