tert-Butyl N-[(4-bromo-2-fluoro-phenyl)methyl]carbamate
98%
- Product Code: 121445
CAS:
864262-97-5
| Molecular Weight: | 304.16 g./mol | Molecular Formula: | C₁₂H₁₅BrFNO₂ |
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| EC Number: | MDL Number: | MFCD08703144 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in organic synthesis as an intermediate for the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a bromo and fluoro substituent on the phenyl ring, makes it valuable for constructing compounds with specific biological activities. It is often employed in the development of drug candidates, where the bromine and fluorine atoms can enhance binding affinity and metabolic stability. Additionally, the tert-butyl carbamate group serves as a protecting group for amines during multi-step synthetic processes, ensuring selective reactivity. Its applications are mainly focused on medicinal chemistry, where it contributes to the creation of novel therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,184.00 |
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| 0.250 | 10-20 days | ฿8,622.00 |
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| 1.000 | 10-20 days | ฿17,253.00 |
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tert-Butyl N-[(4-bromo-2-fluoro-phenyl)methyl]carbamate
This chemical is primarily used in organic synthesis as an intermediate for the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a bromo and fluoro substituent on the phenyl ring, makes it valuable for constructing compounds with specific biological activities. It is often employed in the development of drug candidates, where the bromine and fluorine atoms can enhance binding affinity and metabolic stability. Additionally, the tert-butyl carbamate group serves as a protecting group for amines during multi-step synthetic processes, ensuring selective reactivity. Its applications are mainly focused on medicinal chemistry, where it contributes to the creation of novel therapeutic agents.
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