4-[2-(N-Boc-N-Methyl)aminoethyl]phenylboronic acid
95%
- Product Code: 36819
CAS:
1191062-03-9
| Molecular Weight: | 279.1398 g./mol | Molecular Formula: | C₁₄H₂₂BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27578158 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it acts as a boronic acid reagent. It is valuable for constructing carbon-carbon bonds, especially in the synthesis of complex molecules such as pharmaceuticals, agrochemicals, and advanced materials. The presence of the Boc (tert-butoxycarbonyl) protecting group ensures stability during reactions, while the boronic acid moiety facilitates coupling with aryl or vinyl halides. Its application is also seen in the development of bioactive compounds and in medicinal chemistry research for creating potential drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,609.00 |
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4-[2-(N-Boc-N-Methyl)aminoethyl]phenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it acts as a boronic acid reagent. It is valuable for constructing carbon-carbon bonds, especially in the synthesis of complex molecules such as pharmaceuticals, agrochemicals, and advanced materials. The presence of the Boc (tert-butoxycarbonyl) protecting group ensures stability during reactions, while the boronic acid moiety facilitates coupling with aryl or vinyl halides. Its application is also seen in the development of bioactive compounds and in medicinal chemistry research for creating potential drug candidates.
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