3-Chloro-a-(Boc-amino)-4-fluorobenzeneacetic acid
95%
- Product Code: 41173
CAS:
1038817-56-9
| Molecular Weight: | 303.7139 g./mol | Molecular Formula: | C₁₃H₁₅ClFNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07186276 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of various drugs, including those targeting central nervous system disorders and inflammatory conditions. The Boc (tert-butoxycarbonyl) protecting group in the molecule allows for selective reactions during the synthesis process, ensuring the integrity of the amino group. Its chloro and fluoro substituents contribute to the compound's reactivity and specificity in forming complex organic molecules. Additionally, it is often employed in peptide synthesis and other fine chemical manufacturing processes, where precise molecular modifications are required.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,958.00 |
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3-Chloro-a-(Boc-amino)-4-fluorobenzeneacetic acid
This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of various drugs, including those targeting central nervous system disorders and inflammatory conditions. The Boc (tert-butoxycarbonyl) protecting group in the molecule allows for selective reactions during the synthesis process, ensuring the integrity of the amino group. Its chloro and fluoro substituents contribute to the compound's reactivity and specificity in forming complex organic molecules. Additionally, it is often employed in peptide synthesis and other fine chemical manufacturing processes, where precise molecular modifications are required.
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