9-Borabicyclo[3.3.1]nonane
0.5 M solution in THF, MkSeal
- Product Code: 51265
CAS:
280-64-8
| Molecular Weight: | 122.02 g./mol | Molecular Formula: | C₈H₁₅B |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00074742 | |
| Melting Point: | Boiling Point: | 68-70 °C | |
| Density: | 0.894 g/mL at 25 °C | Storage Condition: | 2~8 ℃ |
Product Description:
9-Borabicyclo[3.3.1]nonane is widely used in organic synthesis as a reagent for hydroboration reactions. It facilitates the addition of boron and hydrogen across carbon-carbon double bonds, which is a key step in the production of alcohols and other functionalized organic compounds. This chemical is particularly valued for its selectivity and efficiency in forming organoboron intermediates, which are crucial in cross-coupling reactions like the Suzuki-Miyaura reaction. Additionally, it is employed in asymmetric synthesis, enabling the creation of chiral molecules with high enantiomeric purity. Its stability and reactivity make it a preferred choice in pharmaceutical and fine chemical industries for constructing complex molecular structures.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | colorless to Light yellow liquid |
| APPEARANCE CLARITY | Clear to Hazy |
| Concentration | 0.45M 0.55M |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 100.000 | 10-20 days | ฿3,200.00 |
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| 500.000 | 10-20 days | ฿11,960.00 |
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| 1000.000 | 10-20 days | ฿19,890.00 |
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9-Borabicyclo[3.3.1]nonane
9-Borabicyclo[3.3.1]nonane is widely used in organic synthesis as a reagent for hydroboration reactions. It facilitates the addition of boron and hydrogen across carbon-carbon double bonds, which is a key step in the production of alcohols and other functionalized organic compounds. This chemical is particularly valued for its selectivity and efficiency in forming organoboron intermediates, which are crucial in cross-coupling reactions like the Suzuki-Miyaura reaction. Additionally, it is employed in asymmetric synthesis, enabling the creation of chiral molecules with high enantiomeric purity. Its stability and reactivity make it a preferred choice in pharmaceutical and fine chemical industries for constructing complex molecular structures.
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