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N32601

Sigma-Aldrich

Norcamphor

98%

Sinônimo(s):

2-Norbornanone, Bicyclo[2.2.1]heptan-2-one

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About This Item

Fórmula empírica (Notação de Hill):
C7H10O
Número CAS:
497-38-1
Peso molecular:
110.15
Beilstein:
1209657
Número CE:
207-846-1
Número MDL:
MFCD00074823
Código UNSPSC:
12352100
ID de substância PubChem:
24897635
NACRES:
NA.22

Ensaio

98%

forma

crystals

pb

168-172 °C (lit.)

pf

93-96 °C (lit.)

cadeia de caracteres SMILES

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

chave InChI

KPMKEVXVVHNIEY-RITPCOANSA-N

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Categorias relacionadas

Pictogramas

Flame
GHS02

Palavra indicadora

Danger

Frases de perigo

H228

Declarações de precaução

P210

Classificações de perigo

Flam. Sol. 1

Código de classe de armazenamento

4.1B - Flammable solid hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

91.4 °F - closed cup

Ponto de fulgor (°C)

33 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

Certificados de análise (COA)

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Bicyclo[2.2.1]hept-2-ene 99%

Sigma-Aldrich

N32407

Bicyclo[2.2.1]hept-2-ene

Lars Goerigk et al.
The journal of physical chemistry. A, 113(4), 767-776 (2008-12-24)
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
Lucyna Balcerzak et al.
Food chemistry, 301, 125283-125283 (2019-08-05)
A small library of 57 low molecular weight oximes was prepared from fragrant aldehydes and ketones, and their olfactory profiles were determined. The most substantive and interesting in terms of the sensory impressions were (+)-isomenthone oxime (fresh, musty, green) and
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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