Molecular structure of B-Iodo-9-BBN, CAS Number: 70145-42-5
B-Iodo-9-BBN (CAS 70145-42-5)
Alternate Names:
9-Iodo-9-borabicyclo[3.3.1]nonane
CAS Number:
70145-42-5
Purity:
≥95%
Molecular Weight:
247.91
Molecular Formula:
C8H14BI
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
B-Iodo-9-BBN, also known as B-iodo-9-borabicyclo[3.3.1]nonane, is a boron-containing compound that features an iodine atom attached to the boron atom. β-Iodo-9-BBN, 1 M in hexanes, is an oxidation product derived from the ketone 9-BBN. It serves as a versatile synthetic reagent for oxidizing halides and enolate olefins. This compound facilitates the synthesis of aryl halides through its reaction with boron enolates, forming covalent bonds between the two components.
B-Iodo-9-BBN (CAS 70145-42-5) References
- A synthesis of aromatic five- and six-membered B-N heterocycles via ring closing metathesis. | Ashe, AJ. and Fang, X. 2000. Org Lett. 2: 2089-91. PMID: 10891237
- Inherently chiral resorcin[4]arenes: a new concept for improving the functionality. | Wiegmann, S. and Mattay, J. 2011. Org Lett. 13: 3226-8. PMID: 21591617
- Palladium(II)-Catalyzed Dehydroboration via Generation of Boron Enolates. | Sakamoto, Y., et al. 2016. Chemistry. 22: 18686-18689. PMID: 27734542
- Synthetic Strategy: Palladium-Catalyzed Dehydrogenation of Carbonyl Compounds. | Hirao, T. 2019. J Org Chem. 84: 1687-1692. PMID: 30668104
- Synthesis of Functionalized Cannabilactones. | Liu, Y., et al. 2020. Molecules. 25: PMID: 32041131
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
B-Iodo-9-BBN, 25 ml | sc-239266 | 25 ml | $196.00 |