Molecular structure of (1R)-(+)-Camphor, CAS Number: 464-49-3
(1R)-(+)-Camphor (CAS 464-49-3)
Alternate Names:
(+)-Camphor; (1R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one
CAS Number:
464-49-3
Purity:
≥98%
Molecular Weight:
152.23
Molecular Formula:
C10H16O
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
(1R)-(+)-Camphor functions as a insect repellent in experimental applications. It acts by disrupting the neurotransmission in insects, leading to their avoidance of the treated area. At the molecular level, (1R)-(+)-Camphor interferes with the function of certain receptors in the insect nervous system, causing a disruption in their ability to detect and respond to environmental cues. This disruption ultimately deters insects from entering or remaining in the treated area, making (1R)-(+)-Camphor useful for studying insect behavior and developing environmentally friendly pest control methods. Its mechanism of action involves interfering with the insect′s sensory perception and neural signaling, making it useful for experimental research in entomology and pest management.
(1R)-(+)-Camphor (CAS 464-49-3) References
- The desymmetrization of bicyclic beta -diketones by an enzymatic retro-Claisen reaction. A new reaction of the crotonase superfamily. | Grogan, G., et al. 2001. J Biol Chem. 276: 12565-72. PMID: 11278926
- Stereoselective hydrocoupling of [(1R)-exo]-3-exo-(diphenylmethyl)bornyl cinnamates by electroreduction. | Kise, N., et al. 2001. Org Lett. 3: 3241-4. PMID: 11594804
- A Highly diastereoselective synthesis of (1R)-(+)-camphor-based chiral allenes and their asymmetric hydroboration-oxidation reactions. | Hung, SC., et al. 2002. J Org Chem. 67: 1308-13. PMID: 11846679
- Chiral tricyclic iminolactone derived from (1R)-(+)-camphor as a glycine equivalent for the asymmetric synthesis of alpha-amino acids. | Xu, PF., et al. 2002. J Org Chem. 67: 2309-14. PMID: 11925246
- P450(camr), a cytochrome P450 catalysing the stereospecific 6- endo-hydroxylation of (1 R)-(+)-camphor. | Grogan, G., et al. 2002. Appl Microbiol Biotechnol. 59: 449-54. PMID: 12172608
- Synthesis and characterization of camphorsulfonyl acetate of cellulose. | Xiao, D., et al. 2004. Carbohydr Res. 339: 1925-31. PMID: 15261585
- Cytochrome P450cam-monoterpene interactions. | Van Roon, A., et al. 2005. SAR QSAR Environ Res. 16: 369-84. PMID: 16234177
- Alternative synthetic route to chiral N-substituted camphor-derived beta-amino alcohols. | Cheng, GI., et al. 2007. Chirality. 19: 235-8. PMID: 17230497
- Toxicity of Myristica fagrans seed compounds against Blattella germanica (Dictyoptera: Blattellidae). | Jung, WC., et al. 2007. J Med Entomol. 44: 524-9. PMID: 17547241
- Electron ionization mass spectral studies of bridgehead-substituted norbornan-2-ones: camphor derivatives. | Teso Vilar, E., et al. 2011. Rapid Commun Mass Spectrom. 25: 395-409. PMID: 21254275
- Identification of camphor oxidation and reduction products in Pseudomonas putida: new activity of the cytochrome P450cam system. | Prasad, B., et al. 2011. J Chem Ecol. 37: 657-67. PMID: 21562741
- The use of deuterated camphor as a substrate in (1)H ENDOR studies of hydroxylation by cryoreduced oxy P450cam provides new evidence of the involvement of compound I. | Davydov, R., et al. 2013. Biochemistry. 52: 667-71. PMID: 23215047
- Modeling the Solubility of Monoterpenoids with Hybrid and Predictive Thermodynamic Tools. | Vilas-Boas, SM., et al. 2023. Ind Eng Chem Res. 62: 5326-5335. PMID: 37014371
- Structural changes in cytochrome P-450cam effected by the binding of the enantiomers (1R)-camphor and (1S)-camphor. | Schulze, H., et al. 1996. Biochemistry. 35: 14127-38. PMID: 8916898
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
(1R)-(+)-Camphor, 5 g | sc-251645 | 5 g | $32.00 |