497-38-1 | Norcamphor

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$14.00	$10.00
5g	95%	in stock	$17.00	$12.00
10g	95%	in stock	$30.00	$21.00
25g	95%	in stock	$65.00	$46.00

Description

• Catalog Number: AG25319
• Chemical Name: Norcamphor
• CAS Number: 497-38-1
• Molecular Formula: C7H10O
• Molecular Weight: 110.1537
• MDL Number: MFCD00074823
• SMILES: C1CC2CC1CC2=O

Computed Properties

• Complexity: 128
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 1
• Undefined Atom Stereocenter Count: 2
• XLogP3: 1

Literature

• Time-dependent fifth-order bands in nominally third-order 2D IR vibrational echo spectra.

  The journal of physical chemistry. A 20110901

• Syntheses and pharmacological evaluations of novel N-substituted bicyclo-heptane-2-amines at N-methyl-D-aspartate receptors.

  Chemical biology & drug design 20110701

• The effect of proton donors on the facial stereoselectivity in SmI2 reduction of norcamphor.

  The Journal of organic chemistry 20110304

• Comparative analysis of IR and vibrational circular dichroism spectra for a series of camphor-related molecules.

  The journal of physical chemistry. A 20091022

• Calculation of electronic circular dichroism spectra with time-dependent double-hybrid density functional theory.

  The journal of physical chemistry. A 20090129

• Comparison of time-dependent density-functional theory and coupled cluster theory for the calculation of the optical rotations of chiral molecules.

  The journal of physical chemistry. A 20080214

• The effect of carbonyl group in the asymmetry of 3,4JCH coupling constants in norbornanones.

  Magnetic resonance in chemistry : MRC 20080201

• Regiodivergent Baeyer-Villiger oxidation of fused ketones by recombinant whole-cell biocatalysts.

  ChemSusChem 20080101

• Sum-over-states calculation of the specific rotations of some substituted oxiranes, chloropropionitrile, ethane, and norbornenone.

  The journal of physical chemistry. A 20061228

• Alkali metal counterion control of enolate protonation stereoselectivity.

  Organic letters 20060622

• Synthesis of (-)-sordarin.

  Journal of the American Chemical Society 20060531

• Ketone synthesis by intramolecular acylation of organorhodium(I) with ester.

  Journal of the American Chemical Society 20050209

• Identification and structure-activity relationship studies of 3-methylene-2-norbornanone as potent anti-proliferative agents presumably working through p53 mediated apoptosis.

  Bioorganic & medicinal chemistry letters 20041115

• Base-promoted reactions of bridged ketones and 1,3- and 1,4-haloalkyl azides: competitive alkylation vs azidation reactions of ketone enolates.

  The Journal of organic chemistry 20040305

• Total synthesis of dumsin. 1. Retrosynthetic strategy and the elaboration of key intermediates from (--)-bornyl acetate.

  The Journal of organic chemistry 20030905

• Role of protein and substrate dynamics in catalysis by Pseudomonas putida cytochrome P450cam.

  Biochemistry 20021210

• Substrates modulate the rate-determining step for CO binding in cytochrome P450cam (CYP101). A high-pressure stopped-flow study.

  European journal of biochemistry 20020601