Pinacol 3-methyl-4-(ethyl carbamoyl) phenylboronic acid
95%
- Product Code: 45435
CAS:
1146157-79-0
| Molecular Weight: | 289.17766 g./mol | Molecular Formula: | C₁₆H₂₄BNO₃ |
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| EC Number: | MDL Number: | MFCD22494147 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate in the development of pharmaceutical compounds. Its boronic acid group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, it is used in the preparation of bioactive molecules and potential drug candidates, particularly in the field of enzyme inhibition and receptor modulation. Its structure allows for selective binding and interaction with biological targets, making it useful in the design of inhibitors for specific enzymes or proteins. The compound’s properties also make it suitable for use in biochemical research, particularly in studies involving boron-containing compounds and their therapeutic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿3,312.00 |
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| 0.100 | 10-20 days | ฿8,892.00 |
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| 0.500 | 10-20 days | ฿26,892.00 |
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Pinacol 3-methyl-4-(ethyl carbamoyl) phenylboronic acid
This chemical is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate in the development of pharmaceutical compounds. Its boronic acid group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, it is used in the preparation of bioactive molecules and potential drug candidates, particularly in the field of enzyme inhibition and receptor modulation. Its structure allows for selective binding and interaction with biological targets, making it useful in the design of inhibitors for specific enzymes or proteins. The compound’s properties also make it suitable for use in biochemical research, particularly in studies involving boron-containing compounds and their therapeutic applications.
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