B-Chlorocatecholborane
>96.0%(T)
- Product Code: 68164
Alias:
2-Chloro-1,3,2-benzenediol borate
CAS:
55718-76-8
| Molecular Weight: | 154.36 g./mol | Molecular Formula: | C₆H₄BClO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00043395 | |
| Melting Point: | 56-58 °C (lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature, inert gas |
Product Description:
B-Chlorocatecholborane is primarily used in organic synthesis as a versatile reagent, particularly in the formation of carbon-boron bonds. It is highly effective in borylation reactions, which are essential for creating organoboron compounds. These compounds are widely employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, to construct complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its reactivity and stability make it a valuable tool in the development of new chemical entities and in the modification of existing compounds for enhanced properties. Additionally, it is utilized in catalytic processes and as a precursor for other boron-containing reagents in synthetic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Light yellow to Light red powder to crystal |
| PURITY | 95.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿7,980.00 |
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| 5.000 | 10-20 days | ฿17,000.00 |
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B-Chlorocatecholborane
B-Chlorocatecholborane is primarily used in organic synthesis as a versatile reagent, particularly in the formation of carbon-boron bonds. It is highly effective in borylation reactions, which are essential for creating organoboron compounds. These compounds are widely employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, to construct complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its reactivity and stability make it a valuable tool in the development of new chemical entities and in the modification of existing compounds for enhanced properties. Additionally, it is utilized in catalytic processes and as a precursor for other boron-containing reagents in synthetic chemistry.
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