4-nitrophenyl N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate
95%
- Product Code: 90474
CAS:
957198-19-5
| Molecular Weight: | 384.19084 g./mol | Molecular Formula: | C₁₉H₂₁BN₂O₆ |
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| EC Number: | MDL Number: | MFCD31583145 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis, particularly in the development of boron-containing compounds. Its structure, featuring a nitrophenyl group and a dioxaborolane moiety, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it serves as an intermediate in the preparation of biologically active compounds, where the boronate ester group can be further functionalized. Its stability and reactivity also make it useful in materials science, particularly in the development of advanced polymers and coatings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿4,923.00 |
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| 0.250 | 10-20 days | ฿19,404.00 |
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4-nitrophenyl N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate
This chemical is primarily used in organic synthesis, particularly in the development of boron-containing compounds. Its structure, featuring a nitrophenyl group and a dioxaborolane moiety, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it serves as an intermediate in the preparation of biologically active compounds, where the boronate ester group can be further functionalized. Its stability and reactivity also make it useful in materials science, particularly in the development of advanced polymers and coatings.
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