(S)-tert-Butyl (1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)carbamate
95%
- Product Code: 37815
CAS:
1171897-03-2
| Molecular Weight: | 347.2600 g./mol | Molecular Formula: | C₁₉H₃₀BNO₄ |
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| EC Number: | MDL Number: | MFCD29912577 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis, particularly in the field of medicinal chemistry, as a key intermediate in the preparation of biologically active compounds. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This reaction is essential in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tert-butyl carbamate (Boc) protecting group ensures selective reactivity during multi-step synthetic processes, allowing for the precise construction of complex molecules. Its application is particularly relevant in the development of drug candidates, where it aids in the creation of diverse and structurally intricate compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,762.00 |
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(S)-tert-Butyl (1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)carbamate
This chemical is primarily used in organic synthesis, particularly in the field of medicinal chemistry, as a key intermediate in the preparation of biologically active compounds. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This reaction is essential in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tert-butyl carbamate (Boc) protecting group ensures selective reactivity during multi-step synthetic processes, allowing for the precise construction of complex molecules. Its application is particularly relevant in the development of drug candidates, where it aids in the creation of diverse and structurally intricate compounds.
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