tert-Butyl (3-amino-2,6-difluorophenyl)carbamate
95%
- Product Code: 36663
CAS:
535170-20-8
| Molecular Weight: | 244.2379 g./mol | Molecular Formula: | C₁₁H₁₄F₂N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13182479 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key building block in the production of compounds with potential therapeutic applications, especially in the field of medicinal chemistry. Its structure, featuring amino and difluoro groups, makes it valuable for creating molecules with specific biological activities, such as enzyme inhibition or receptor modulation. Additionally, it is employed in research settings for the design and optimization of drug candidates, particularly those targeting diseases like cancer or neurological disorders. Its stability and reactivity also make it suitable for use in organic synthesis and combinatorial chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $41.04 |
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tert-Butyl (3-amino-2,6-difluorophenyl)carbamate
This chemical is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key building block in the production of compounds with potential therapeutic applications, especially in the field of medicinal chemistry. Its structure, featuring amino and difluoro groups, makes it valuable for creating molecules with specific biological activities, such as enzyme inhibition or receptor modulation. Additionally, it is employed in research settings for the design and optimization of drug candidates, particularly those targeting diseases like cancer or neurological disorders. Its stability and reactivity also make it suitable for use in organic synthesis and combinatorial chemistry.
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