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N32601

Norcamphor

Name: Norcamphor
Brand: ALDRICH

98%

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):

C₇H₁₀O

CAS Number:

497-38-1

Molecular Weight:

110.15

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24897635

EC Number:

207-846-1

Beilstein/REAXYS Number:

1209657

MDL number:

MFCD00074823

Assay:

98%

Form:

crystals

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Properties

Quality Level

100

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

Description

pictograms

GHS02

signalword

Danger

hcodes

H228

pcodes

P210

Hazard Classifications

Flam. Sol. 1

Storage Class

4.1B - Flammable solid hazardous materials

wgk

WGK 3

flash_point_f

91.4 °F - closed cup

flash_point_c

33 °C - closed cup

ppe

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

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Step-scan time-resolved FTIR spectroscopy of cytochrome P-450cam carbon monoxide complex: a salt link involved in the ligand-rebinding process.

J Contzen et al.

Biochemistry, 37(13), 4317-4324 (1998-04-29)

Step-scan time-resolved Fourier transform infrared spectroscopy with a time resolution of 5 micros was applied to the carbon monoxide complex of cytochrome P-450cam (CYP101) to study the bimolecular ligand-rebinding process after flash photolysis. Spectral changes in the CO ligand stretch

Theoretical study of the product specificity in the hydroxylation of camphor, norcamphor, 5,5-difluorocamphor, and pericyclocamphanone by cytochrome P-450cam.

J R Collins et al.

The Journal of biological chemistry, 263(7), 3164-3170 (1988-03-05)

The hydroxylations of d-camphor, norcamphor, pericyclocamphanone, and 5,5-difluorocamphor by cytochrome P-450cam have been examined using theoretical methods to identify and characterize properties which determine product specificity. Experimental results indicate that each molecule is hydroxylated with quite different regio-specificity when metabolized

Substrate mobility in a deeply buried active site: analysis of norcamphor bound to cytochrome P-450cam as determined by a 201-psec molecular dynamics simulation.

M B Bass et al.

Proteins, 13(1), 26-37 (1992-05-01)

While cytochrome P-450cam catalyzes the hydroxylation of camphor to 5-exo-hydroxycamphor with 100% stereospecificity, norcamphor is hydroxylated by this enzyme yielding 45% 5-exo-, 47% 6-exo-, and 8% 3-exo-hydroxynorcamphor (Atkins, W.M., Sligar, S.G., J. Am. Chem. Soc. 109:3754-3760, 1987). The present study

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Global Trade Item Number

SKU	GTIN
N32601-25G	04061831827361
N32601-100G	04061834115908
N32601-5G	04061834115915