tert-Butyl (4-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate
98%
- Product Code: 113295
CAS:
1080573-28-9
| Molecular Weight: | 353.65 g./mol | Molecular Formula: | C₁₇H₂₅BClNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23379564 | |
| Melting Point: | Boiling Point: | 410.4±40.0 °C(Predicted) | |
| Density: | 1.14±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This reaction is crucial in creating complex organic molecules, including active pharmaceutical ingredients (APIs) and biologically active compounds. Additionally, the carbamate group provides stability and can act as a protective group for amines during synthetic processes, enabling selective reactions in multi-step syntheses. Its applications are particularly significant in the production of targeted drugs and advanced materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,647.00 |
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| 0.250 | 10-20 days | ฿2,790.00 |
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| 1.000 | 10-20 days | ฿7,515.00 |
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tert-Butyl (4-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate
This chemical is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This reaction is crucial in creating complex organic molecules, including active pharmaceutical ingredients (APIs) and biologically active compounds. Additionally, the carbamate group provides stability and can act as a protective group for amines during synthetic processes, enabling selective reactions in multi-step syntheses. Its applications are particularly significant in the production of targeted drugs and advanced materials.
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