N32601
Norcamphor
98%
Sinónimos:
2-Norbornanone, Bicyclo[2.2.1]heptan-2-one
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About This Item
Fórmula empírica (notación de Hill):
C7H10O
Número de CAS:
Peso molecular:
110.15
Beilstein/REAXYS Number:
1209657
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
98%
form
crystals
bp
168-172 °C (lit.)
mp
93-96 °C (lit.)
SMILES string
O=C1C[C@@H]2CC[C@H]1C2
InChI
1S/C7H10O/c8-7-4-5-1-2-6(7)3-5/h5-6H,1-4H2/t5-,6+/m1/s1
InChI key
KPMKEVXVVHNIEY-RITPCOANSA-N
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Time-dependent double-hybrid density functional theory is applied to the calculation of the electronic circular dichroism (CD) spectra of molecules. The TD-B2PLYP method is based on vertical excitation energies obtained from its hybrid-GGA part B2LYP in a conventional TD-DFT linear response
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M D Paulsen et al.
Protein science : a publication of the Protein Society, 2(3), 357-365 (1993-03-01)
Cytochrome P450cam (P450CIA1) catalyzes the hydroxylation of camphor and several substrate analogues such as norcamphor and 1-methyl-norcamphor. Hydroxylation was found experimentally at the 3, 5, and 6 positions of norcamphor, but only at the 5 and 6 positions of 1-methyl-norcamphor.
W M Atkins et al.
Biochemistry, 27(5), 1610-1616 (1988-03-08)
The kinetics of NADH consumption, oxygen uptake, and hydrogen peroxide production have been studied for norcamphor metabolism by cytochrome P-450cam. The kinetic deuterium isotope effects on these processes, with specifically deuteriated norcamphor, are 0.77, 1.22, and 1.16, respectively. Steady-state UV-visible
Sarasij Kumar Upadhyay et al.
The Journal of organic chemistry, 76(5), 1355-1360 (2011-01-22)
The endo/exo product ratio in the reactions of SmI(2) with norcamphor in the presence of various proton donors was determined. The effect of MeOH, EtOH, trifluoroethanol (TFE), ethylene glycol (EG), and water was investigated at various concentrations of these proton
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