2-Aminobenzeneboronic acid pinacol ester
97%
- Product Code: 67415
Alias:
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
CAS:
191171-55-8
Molecular Weight: | 219.09 g./mol | Molecular Formula: | C₁₂H₁₈BNO₂ |
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EC Number: | MDL Number: | MFCD02179448 | |
Melting Point: | 63-68 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | 2~8°C |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other therapeutic agents. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. This compound is also utilized in the preparation of boron-containing materials for optoelectronic applications. Additionally, it serves as a building block in the creation of sensors and probes for detecting biological molecules due to its boronic acid functionality.
Product Specification:
Test | Specification |
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Carbon | 62.5-69.1 |
Nitrogen | 6-6.7 |
Purity (HPLC) | 97-100 |
Melting Point | 64-70 |
Appearance | White to orange to brown powder, crystals or chunks |
Infrared Spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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1g | 10-20 days | ฿540.00 |
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5g | 10-20 days | ฿2,400.00 |
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25g | 10-20 days | ฿11,700.00 |
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100g | 10-20 days | ฿46,740.00 |
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2-Aminobenzeneboronic acid pinacol ester
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other therapeutic agents. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. This compound is also utilized in the preparation of boron-containing materials for optoelectronic applications. Additionally, it serves as a building block in the creation of sensors and probes for detecting biological molecules due to its boronic acid functionality.
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