tert-Butyl (6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-yl)carbamate
97%
- Product Code: 37087
CAS:
1312611-41-8
| Molecular Weight: | 369.2623 g./mol | Molecular Formula: | C₂₁H₂₈BNO₄ |
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| EC Number: | MDL Number: | MFCD13191643 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the tert-butyl carbamate group serves as a protective group for amines, allowing selective reactions to occur without interference. Its stability and reactivity make it a versatile intermediate in medicinal chemistry for the development of drug candidates and bioactive compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,012.00 |
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tert-Butyl (6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-yl)carbamate
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the tert-butyl carbamate group serves as a protective group for amines, allowing selective reactions to occur without interference. Its stability and reactivity make it a versatile intermediate in medicinal chemistry for the development of drug candidates and bioactive compounds.
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