2-Amino-5-bromo-3-fluorobenzoic acid

97%

  • Product Code: 116303
  CAS:    874784-14-2
Molecular Weight: 234.02 g./mol Molecular Formula: C₇H₅BrFNO₂
EC Number: MDL Number: MFCD04035659
Melting Point: Boiling Point: 321.7±42.0°C at 760 mmHg
Density: Storage Condition: Room temperature, dry and sealed
Product Description: 2-Amino-5-bromo-3-fluorobenzoic acid is primarily used in organic synthesis as a building block for the development of more complex chemical compounds. Its structure, featuring both amino and halogen substituents, makes it a versatile intermediate in the synthesis of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs). The compound is often employed in the preparation of heterocyclic compounds, which are crucial in drug discovery and development. Additionally, its halogenated aromatic ring allows for further functionalization, enabling the production of specialized chemicals used in agrochemicals and material science. Its unique properties also make it valuable in research settings for studying reaction mechanisms and developing new synthetic methodologies.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days €16.38
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1.000 10-20 days €41.79
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5.000 10-20 days €153.38
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2-Amino-5-bromo-3-fluorobenzoic acid
2-Amino-5-bromo-3-fluorobenzoic acid is primarily used in organic synthesis as a building block for the development of more complex chemical compounds. Its structure, featuring both amino and halogen substituents, makes it a versatile intermediate in the synthesis of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs). The compound is often employed in the preparation of heterocyclic compounds, which are crucial in drug discovery and development. Additionally, its halogenated aromatic ring allows for further functionalization, enabling the production of specialized chemicals used in agrochemicals and material science. Its unique properties also make it valuable in research settings for studying reaction mechanisms and developing new synthetic methodologies.
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