Borane triethylamine complex
90%
- Product Code: 63418
CAS:
1722-26-5
| Molecular Weight: | 115.02 g./mol | Molecular Formula: | C₆H₁₈BN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00012423 | |
| Melting Point: | -4°C (Lit.) | Boiling Point: | 97°C 12mm Hg (Lit.) |
| Density: | 0.7770g/ml | Storage Condition: | room temperature |
Product Description:
Borane triethylamine complex is widely used as a reducing agent in organic synthesis. It is particularly effective in the reduction of carboxylic acids to their corresponding alcohols, offering a milder alternative to other reducing agents like lithium aluminum hydride. Additionally, it is employed in the selective reduction of nitriles to primary amines, a crucial step in the production of various pharmaceuticals and agrochemicals. The complex is also utilized in hydroboration reactions, where it facilitates the addition of boron-hydrogen bonds to alkenes, forming organoboron compounds that are valuable intermediates in further synthetic transformations. Its stability and ease of handling make it a preferred choice in laboratory and industrial settings for these applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Almost colorless clear liquid |
| PURITY | 89.5-100 |
| Carbon NMR Spectrum | Conforms to Structure |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿1,020.00 |
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| 25.000 | 10-20 days | ฿3,110.00 |
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Borane triethylamine complex
Borane triethylamine complex is widely used as a reducing agent in organic synthesis. It is particularly effective in the reduction of carboxylic acids to their corresponding alcohols, offering a milder alternative to other reducing agents like lithium aluminum hydride. Additionally, it is employed in the selective reduction of nitriles to primary amines, a crucial step in the production of various pharmaceuticals and agrochemicals. The complex is also utilized in hydroboration reactions, where it facilitates the addition of boron-hydrogen bonds to alkenes, forming organoboron compounds that are valuable intermediates in further synthetic transformations. Its stability and ease of handling make it a preferred choice in laboratory and industrial settings for these applications.
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