5771-58-4 Usage
Uses
Used in Pharmaceutical Research:
Bicyclo[4.1.0]heptan-2-one is used as a research compound for investigating the anti-inflammatory and analgesic potentials of Habenaria digitata, a plant species with potential medicinal properties. Its unique structure and reactivity contribute to the development of new drugs and therapies for pain relief and inflammation management.
Used in Chemical Synthesis:
Bicyclo[4.1.0]heptan-2-one can be utilized as an intermediate in the synthesis of various organic compounds, particularly those with potential applications in the pharmaceutical, agrochemical, and materials science industries. Its versatile structure allows for further functionalization and modification to create new molecules with desired properties.
Used in Analytical Chemistry:
As a reference compound, Bicyclo[4.1.0]heptan-2-one can be employed in analytical chemistry for the calibration of instruments, method development, and validation. Its distinct chemical properties make it a useful standard for comparing and analyzing other compounds in various research and industrial applications.
Synthesis Reference(s)
Tetrahedron Letters, 31, p. 6969, 1990 DOI: 10.1016/S0040-4039(00)97218-6
Check Digit Verification of cas no
The CAS Registry Mumber 5771-58-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,7 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5771-58:
(6*5)+(5*7)+(4*7)+(3*1)+(2*5)+(1*8)=114
114 % 10 = 4
So 5771-58-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O/c8-7-3-1-2-5-4-6(5)7/h5-6H,1-4H2
5771-58-4Relevant academic research and scientific papers
Cage escape competes with geminate recombination during alkane hydroxylation by the diiron oxygenase AlkB
Austin, Rachel N.,Luddy, Kate,Erickson, Karla,Pender-Cudlip, Marilla,Bertrand, Erin,Deng, Dayi,Buzdygon, Ryan S.,Van Beilen, Jan B.,Groves, John T.
supporting information; experimental part, p. 5232 - 5234 (2009/04/04)
(Chemical Presented) AlkBstops the radical clock: Three structurally analogous radical-clock substrates with a large span in their rearrangement rates are hydroxylated by AlkB to afford similar amounts of rearranged (2) and unrearranged products (1). Such a result is in accord with radical rebound competing with cage escape of the geminate substrate radical. The results show that radical clocks can measure both the radical lifetime and the kinetics of cage escape.
