CAS 13173-09-6: Bicyclo(3.2.0)hept-2-en-6-one,96%

(+/-) - cis-Bicyclo[3,2,0]hept-2-en-6-one is a compound that can be synthesized by using two different methods. The first method involves the use of phase chromatography and gel chromatography to separate the reaction products. The second method involves kinetic measurements, which are used to optimize the process. Dehydrogenase enzymes are used in this process as they catalyze hydrogen transfer reactions. Chemometric analysis was also used to determine kinetics and thermodynamic data for the synthesis of (+/-) - cis-Bicyclo[3,2,0]hept-2-en-6-one. Molecular modelling and chemical reactions were also studied in order to find an enantiomer of (+/-) - cis-Bicyclo[3,2,0]hept-2-en 6 one. This compound is often used in asymmetric synthesis because it has a cyclopentan

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. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Bicyclo[3.2.0]Hept-2-En-6-One