2-Amino-6-bromo-3-chloro-5-fluorobenzoic acid
97%
- Product Code: 116354
CAS:
1513119-35-1
| Molecular Weight: | 268.47 g./mol | Molecular Formula: | C₁₀H₁₁FO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23795936 | |
| Melting Point: | Boiling Point: | 342.8±42.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
This chemical is primarily used in organic synthesis as a building block for the development of more complex molecules. It serves as a key intermediate in the production of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that require halogenated aromatic compounds. Its unique combination of functional groups makes it valuable for creating compounds with specific biological activities, such as antimicrobial or anti-inflammatory agents. Additionally, it is utilized in research and development for designing and testing new drug candidates, especially in the field of medicinal chemistry. Its halogen substituents also make it suitable for use in cross-coupling reactions, which are essential in constructing diverse organic frameworks.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $46.37 |
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| 0.250 | 10-20 days | $69.37 |
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| 1.000 | 10-20 days | $173.07 |
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2-Amino-6-bromo-3-chloro-5-fluorobenzoic acid
This chemical is primarily used in organic synthesis as a building block for the development of more complex molecules. It serves as a key intermediate in the production of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that require halogenated aromatic compounds. Its unique combination of functional groups makes it valuable for creating compounds with specific biological activities, such as antimicrobial or anti-inflammatory agents. Additionally, it is utilized in research and development for designing and testing new drug candidates, especially in the field of medicinal chemistry. Its halogen substituents also make it suitable for use in cross-coupling reactions, which are essential in constructing diverse organic frameworks.
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