1-pinacolato-2-(1,8)diamo-naphthalenylborane
97%
- Product Code: 91242
CAS:
1214264-88-6
| Molecular Weight: | 293.96 g./mol | Molecular Formula: | C₁₆H₂₀B₂N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27980593 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, stored in inert gas |
Product Description:
Used as a versatile reagent in organic synthesis, particularly in the formation of carbon-boron bonds. It plays a key role in Suzuki-Miyaura cross-coupling reactions, enabling the creation of complex organic molecules. Its application extends to the development of pharmaceuticals, agrochemicals, and advanced materials. The compound is also employed in catalytic systems for selective transformations, enhancing efficiency in synthetic pathways. Its stability and reactivity make it a valuable tool in modern synthetic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | off-white powder |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿550.00 |
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| 1.000 | 10-20 days | ฿2,150.00 |
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| 5.000 | 10-20 days | ฿9,740.00 |
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1-pinacolato-2-(1,8)diamo-naphthalenylborane
Used as a versatile reagent in organic synthesis, particularly in the formation of carbon-boron bonds. It plays a key role in Suzuki-Miyaura cross-coupling reactions, enabling the creation of complex organic molecules. Its application extends to the development of pharmaceuticals, agrochemicals, and advanced materials. The compound is also employed in catalytic systems for selective transformations, enhancing efficiency in synthetic pathways. Its stability and reactivity make it a valuable tool in modern synthetic chemistry.
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