tert-butyl N-[2-([3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamoylamino)ethyl]carbamate
95%
- Product Code: 218344
CAS:
1036990-28-9
| Molecular Weight: | 405.29618 g./mol | Molecular Formula: | C₂₀H₃₂BN₃O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32206586 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature |
Product Description:
Widely used in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for constructing biaryl and heterobiaryl systems in pharmaceutical and agrochemical research. The presence of the boronate ester group enables efficient palladium-catalyzed coupling with aryl halides, allowing for the formation of carbon-carbon bonds under mild conditions. Its protected amine functionalities make it suitable for peptide modification and the development of complex nitrogen-containing molecules. Commonly employed in medicinal chemistry for library synthesis and structure-activity relationship studies, it supports the rapid assembly of drug-like scaffolds. Additionally, it is utilized in materials science for designing conjugated systems in organic electronics.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿23,200.00 |
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| 1g | 10-20 days | ฿56,000.00 |
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tert-butyl N-[2-([3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamoylamino)ethyl]carbamate
Widely used in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for constructing biaryl and heterobiaryl systems in pharmaceutical and agrochemical research. The presence of the boronate ester group enables efficient palladium-catalyzed coupling with aryl halides, allowing for the formation of carbon-carbon bonds under mild conditions. Its protected amine functionalities make it suitable for peptide modification and the development of complex nitrogen-containing molecules. Commonly employed in medicinal chemistry for library synthesis and structure-activity relationship studies, it supports the rapid assembly of drug-like scaffolds. Additionally, it is utilized in materials science for designing conjugated systems in organic electronics.
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