N32601
Norcamphor
98%
Synonym(s):
2-Norbornanone, Bicyclo[2.2.1]heptan-2-one
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All Photos(3)
About This Item
Empirical Formula (Hill Notation):
C7H10O
CAS Number:
Molecular Weight:
110.15
Beilstein:
1209657
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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![Bicyclo[2.2.1]hept-2-ene 99%](/deepweb/assets/sigmaaldrich/product/structures/270/492/95fd4909-6108-4858-8c94-609b54387149/640/95fd4909-6108-4858-8c94-609b54387149.png)
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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Related Categories
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Sol. 1
Storage Class Code
4.1B - Flammable solid hazardous materials
WGK
WGK 3
Flash Point(F)
91.4 °F - closed cup
Flash Point(C)
33 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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.
Mohammed A Alamri et al.
Medicinal chemistry (Shariqah (United Arab Emirates)), 16(2), 192-201 (2019-03-05)
Novel bicycloheptylamines were designed and synthesized. These compounds were found to be selective for sigma-2 receptors. These receptors have been found to be up to 10 fold over-expressed in certain cancer cell lines, leading to investigation of possible uses as
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
Sergio Abbate et al.
The journal of physical chemistry. A, 113(42), 11390-11405 (2009-09-30)
The absorption spectra and vibrational circular dichroism (VCD) spectra in the mid-IR range 1600-950 cm(-1) of 10 camphor-related compounds have been recorded and compared to DFT calculated spectra at the B3PW91/TZ2P level and have been examined together with the corresponding
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