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| | 9-BROMO-9-BORABICYCLO[3.3.1]NONANE Basic information |
| Product Name: | 9-BROMO-9-BORABICYCLO[3.3.1]NONANE | | Synonyms: | B-BROMO-9-BBN;B-BROMO-9-BBN 1.0M SOLUTION IN &;B-BROMO-9-BBN, 1.0M SOLUTION IN DICHLOROMETHANE;9-Bromo-9-borabicyclo[3.3.1]nonane solution;B-Bromo-9-BBN solution;9-BROMO-9-BORABICYCLO[3.3.1]NONANE;B-Bromo-9-borabicyclo[3.3.1]nonane;9-Borabicyclo[3.3.1]nonane, 9-bromo- | | CAS: | 22086-45-9 | | MF: | C8H14BBr | | MW: | 200.91 | | EINECS: | | | Product Categories: | | | Mol File: | 22086-45-9.mol | ![9-BROMO-9-BORABICYCLO[3.3.1]NONANE Structure](CAS/GIF/22086-45-9.gif) |
| | 9-BROMO-9-BORABICYCLO[3.3.1]NONANE Chemical Properties |
| Boiling point | 54-59 °C(Press: 0.3-0.4 Torr) | | density | 1.315 g/mL at 25 °C | | Fp | -17 °C | | solubility | sol pentane, CH2Cl2; dec ethers, alcohols |
| | 9-BROMO-9-BORABICYCLO[3.3.1]NONANE Usage And Synthesis |
| Uses | 9-BROMO-9-BORABICYCLO[3.3.1]NONANE is a selective reagent for the cleavage of ethers and deoxygenation of sulfoxides; adds regioselectively and stereoselectively to terminal alkynes; undergoes conjugate addition to α,β-unsaturated ketones; converts vinyltins to vinylboranes. | | storage | 9-BROMO-9-BORABICYCLO[3.3.1]NONANE is pyrophoric and reacts violently with moisture and protic solvents. Individuals should thoroughly familiarize themselves with the special handling techniques required for such reagents prior to use. Use in a well-ventilated fume hood. |
| | 9-BROMO-9-BORABICYCLO[3.3.1]NONANE Preparation Products And Raw materials |
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