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N32601 Aldrich

Norcamphor

98%

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

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Properties

Related Categories Building Blocks, C7 to C8, Carbonyl Compounds, Chemical Synthesis, Ketones,
assay   98%
bp   168-172 °C(lit.)
mp   93-96 °C(lit.)

Description

Frequently Asked Questions

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Packaging

5, 25, 100 g in glass bottle

Price and Availability

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Safety & Documentation

Safety Information

Symbol 
GHS02  GHS02
Signal word 
Danger
Hazard statements 
Precautionary statements 
RIDADR 
UN 1325 4.1 / PGII
WGK Germany 
3
RTECS 
RB7680000
Flash Point(F) 
91.4 °F
Flash Point(C) 
33 °C

Protocols & Articles

Peer-Reviewed Papers

References

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Regiodivergent Baeyer-Villiger oxidation of fused ketones by recombinant whole-cell biocatalysts. Mihovilovic MD, Kapitán P, and Kapitánová P ChemSusChem 1(1-2), 143-8, (2008)

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The effect of proton donors on the facial stereoselectivity in SmI2 reduction of norcamphor. Upadhyay SK and Hoz S J. Org. Chem. 76(5), 1355-60, (2011)

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Calculation of electronic circular dichroism spectra with time-dependent double-hybrid density functional theory. Goerigk L and Grimme S J. Phys. Chem. A 113(4), 767-76, (2009)

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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. Bass MB, Paulsen MD, and Ornstein RL Proteins 13(1), 26-37, (1992)

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The structural basis for substrate-induced changes in redox potential and spin equilibrium in cytochrome P-450CAM. Raag R and Poulos TL Biochemistry 28(2), 917-22, (1989)

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Theoretical study of the product specificity in the hydroxylation of camphor, norcamphor, 5,5-difluorocamphor, and pericyclocamphanone by cytochrome P-450cam. Collins JR and Loew GH J. Biol. Chem. 263(7), 3164-70, (1988)

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Stereoselective hydroxylation of norcamphor by cytochrome P450cam. Experimental verification of molecular dynamics simulations. Loida PJ, Sligar SG, Paulsen MD, et al. J. Biol. Chem. 270(10), 5326-30, (1995)

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Deuterium isotope effects in norcamphor metabolism by cytochrome P-450cam: kinetic evidence for the two-electron reduction of a high-valent iron-oxo intermediate. Atkins WM and Sligar SG Biochemistry 27(5), 1610-6, (1988)

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Substrates modulate the rate-determining step for CO binding in cytochrome P450cam (CYP101). A high-pressure stopped-flow study. Jung C, Bec N, and Lange R Eur. J. Biochem. 269(12), 2989-96, (2002)

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Comparative analysis of IR and vibrational circular dichroism spectra for a series of camphor-related molecules. Abbate S, Burgi LF, Gangemi F, et al. J. Phys. Chem. A 113(42), 11390-405, (2009)

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Controlling the regiospecificity and coupling of cytochrome P450cam: T185F mutant increases coupling and abolishes 3-hydroxynorcamphor product. Paulsen MD, Filipovic D, Sligar SG, et al. Protein Sci. 2(3), 357-65, (1993)

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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. Contzen J and Jung C Biochemistry 37(13), 4317-24, (1998)

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Role of protein and substrate dynamics in catalysis by Pseudomonas putida cytochrome P450cam. Prasad S and Mitra S Biochemistry 41(49), 14499-508, (2002)

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Time-dependent fifth-order bands in nominally third-order 2D IR vibrational echo spectra. Thielges MC and Fayer MD J. Phys. Chem. A 115(34), 9714-23, (2011)

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Conformational relaxation in hemoproteins: the cytochrome P-450cam case. Tetreau C, Tourbez M, and Lavalette D Biochemistry 39(46), 14219-31, (2000)

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Beil. 7,IV,139

Aldrich MSDS 1, 1393:D / Corp MSDS 1 (2), 2624:A / FT-IR 1 (1), 440:B / FT-IR 2 (1), 683:D / FT-NMR 1 (1), 678:A / IR-Spectra (3), 260:G / IR-Spectra (2), 233:B / NMR-Reference 2 (1), 402:C / RegBook 1 (1), 475:D / Sax 6, 2070 / Sigma FT-IR 1 (2), 806:A / Structure Index 1, 68:C:1 / Vapor Phase 3, 526:B

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