(+)-3-Bromocamphor (CAS 10293-06-8)
(+)-3-Bromocamphor (CAS:
10293-06-8) has molecular formula C10H15BrO and molecular weight 231.13 g/mol. This compound has been the subject of numerous scientific investigations due to its structural features and practical utility in synthetic chemistry and industrial processes. View product details →
Product Background
This comprehensive research profile examines the scientific literature surrounding (+)-3-Bromocamphor.
Key Research Findings
- Our results indicate that the DEA signals stem exclusively from halide ions produced by the fast dissociation of low-lying sigma* anion states.
- We found that the odors of the Z-isomers were similar to those of the corresponding saturated compounds, but clearly different from the odors of the corresponding E-isomers .
Detailed Literature Analysis
Below are the top-ranked research papers for (+)-3-Bromocamphor, presented with bibliographic details and scientific abstracts.
Synthetic Chemistry
1. Anion states of halocamphor molecules: insights into chirally sensitive dissociative electron attachment.
Recent measurements of spin-polarized electron collisions with halocamphor molecules have observed intriguing trends in their dissociative electron attachment (DEA) chiral asymmetries. While the differences between the DEA asymmetries of 3-bromocamphor (3BrC) and 3-iodocamphor (3IC) were consistent with the larger atomic number of iodine, the e
2. Structure-odor relationships of α-santalol derivatives with modified side chains.
(Z)-alpha-Santalol, which has a unique woody odor, is a main constituent of sandalwood essential oil. We investigated the structure-odor relationship of (Z)-alpha-santalol and its derivatives, focusing on the relationship between the structure of the side chain and the odor of the compounds. Various alpha-santalol derivatives (aldehydes, format
Other Research
3. Discrimination of chiral guests by chiral channels: variable temperature studies by SXRD and solid state 13C NMR of the deoxycholic acid complexes of camphorquinone and endo-3-bromocamphor.
3alpha,12alpha-dihydroxy-5beta-cholan-24-oic acid (deoxycholic acid DCA) is able to discriminate between the R- and S-enantiomers of camphorquinone and endo-(+)-3-bromocamphor and select only the S-enantiomers from a racemic mixture. DCA forms novel well ordered 1:1 adducts with (1S)-(+)-camphorquinone and (1S)-endo-(-)-3-bromocamphor, both of
Conclusion
The research literature on (+)-3-Bromocamphor demonstrates sustained scientific interest, with publications continuing through 0. The compound serves as an important building block in synthetic chemistry and has been explored for various applications. Researchers and industrial users can view detailed specifications or submit an inquiry for pricing and availability.
Data Sources: PubMed/MEDLINE, CrossRef. 3 papers analyzed. Last updated: 2026-05-25. This article is automatically generated from peer-reviewed research data.