Benzyl ((benzyloxy)carbonyl)(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenethyl)carbamate
97%
- Product Code: 42333
CAS:
2304635-13-8
| Molecular Weight: | 515.4051 g./mol | Molecular Formula: | C₃₀H₃₄BNO₆ |
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| EC Number: | MDL Number: | MFCD31556220 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in peptide chemistry and medicinal research. It serves as a protected intermediate in the synthesis of complex molecules, enabling the controlled introduction of functional groups. The presence of the boronate ester group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds in pharmaceutical and material science applications. Additionally, its benzyloxycarbonyl (Cbz) protecting group is commonly employed to safeguard amines during multi-step synthetic processes, ensuring selective reactivity and stability. Its role in the development of bioactive compounds and drug candidates highlights its importance in advancing therapeutic innovations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $720.66 |
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Benzyl ((benzyloxy)carbonyl)(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenethyl)carbamate
This compound is primarily utilized in the field of organic synthesis, particularly in peptide chemistry and medicinal research. It serves as a protected intermediate in the synthesis of complex molecules, enabling the controlled introduction of functional groups. The presence of the boronate ester group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds in pharmaceutical and material science applications. Additionally, its benzyloxycarbonyl (Cbz) protecting group is commonly employed to safeguard amines during multi-step synthetic processes, ensuring selective reactivity and stability. Its role in the development of bioactive compounds and drug candidates highlights its importance in advancing therapeutic innovations.
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