(2-Isopropoxyphenyl)boronic acid
97%
- Product Code: 67364
CAS:
138008-97-6
| Molecular Weight: | 180.01 g./mol | Molecular Formula: | C₉H₁₃BO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03427050 | |
| Melting Point: | 30-35°C | Boiling Point: | 199°C |
| Density: | Storage Condition: | 2-8°C |
Product Description:
(2-Isopropoxyphenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate, enabling the introduction of the (2-isopropoxyphenyl) group into complex molecules. It is also used in the development of boron-containing compounds for medicinal chemistry, where boron’s unique properties can enhance drug efficacy and selectivity. Additionally, it finds applications in the synthesis of organic electronic materials, contributing to the advancement of OLEDs and other optoelectronic devices.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿684.00 |
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| 5.000 | 10-20 days | ฿2,880.00 |
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(2-Isopropoxyphenyl)boronic acid
(2-Isopropoxyphenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate, enabling the introduction of the (2-isopropoxyphenyl) group into complex molecules. It is also used in the development of boron-containing compounds for medicinal chemistry, where boron’s unique properties can enhance drug efficacy and selectivity. Additionally, it finds applications in the synthesis of organic electronic materials, contributing to the advancement of OLEDs and other optoelectronic devices.
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