4-Oxo-4-((3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)amino)butanoic acid
96%
- Product Code: 118972
CAS:
1030269-28-3
| Molecular Weight: | 319.16 g./mol | Molecular Formula: | C₁₆H₂₂BNO₅ |
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| EC Number: | MDL Number: | MFCD06795662 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the development of boron-containing compounds. Its structure, featuring a dioxaborolane group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the preparation of biologically active molecules, enabling the incorporation of boron into complex organic frameworks. Additionally, its reactive functional groups allow for further derivatization, making it a versatile building block in medicinal chemistry for drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | ฿1,260.00 |
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| 1.000 | 10-20 days | ฿3,402.00 |
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| 5.000 | 10-20 days | ฿11,907.00 |
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4-Oxo-4-((3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)amino)butanoic acid
This chemical is primarily utilized in organic synthesis, particularly in the development of boron-containing compounds. Its structure, featuring a dioxaborolane group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the preparation of biologically active molecules, enabling the incorporation of boron into complex organic frameworks. Additionally, its reactive functional groups allow for further derivatization, making it a versatile building block in medicinal chemistry for drug discovery and development.
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