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![双环[3.3.1]壬基-9-酮 ≥98%](/deepweb/assets/sigmaaldrich/product/structures/270/852/60661ded-13fb-4fc7-af36-a381880070a5/640/60661ded-13fb-4fc7-af36-a381880070a5.png)
化驗
98%
形狀
crystals
bp
168-172 °C (lit.)
mp
93-96 °C (lit.)
SMILES 字串
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 密鑰
KPMKEVXVVHNIEY-RITPCOANSA-N
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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.
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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
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