3-(2-Bromo-4-fluorophenyl)propionic acid
97%
- Product Code: 117396
CAS:
174603-55-5
Molecular Weight: | 247.06 g./mol | Molecular Formula: | C₉H₈BrFO₂ |
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EC Number: | MDL Number: | MFCD06656907 | |
Melting Point: | Boiling Point: | 331.4±27.0°C at 760 mmHg | |
Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and biologically active molecules. Its structure, featuring both bromo and fluoro substituents, makes it a valuable building block for the development of compounds with potential therapeutic properties. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to create complex aromatic systems. Additionally, its carboxylic acid group allows for further functionalization, enabling the synthesis of esters, amides, or other derivatives. This chemical is particularly relevant in medicinal chemistry for designing drug candidates targeting specific diseases, including cancer and inflammatory disorders. Its unique halogenated aromatic ring also contributes to its use in materials science, where it can be incorporated into polymers or small molecules for advanced applications.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,908.00 |
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0.250 | 10-20 days | ฿3,150.00 |
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1.000 | 10-20 days | ฿6,237.00 |
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3-(2-Bromo-4-fluorophenyl)propionic acid
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and biologically active molecules. Its structure, featuring both bromo and fluoro substituents, makes it a valuable building block for the development of compounds with potential therapeutic properties. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to create complex aromatic systems. Additionally, its carboxylic acid group allows for further functionalization, enabling the synthesis of esters, amides, or other derivatives. This chemical is particularly relevant in medicinal chemistry for designing drug candidates targeting specific diseases, including cancer and inflammatory disorders. Its unique halogenated aromatic ring also contributes to its use in materials science, where it can be incorporated into polymers or small molecules for advanced applications.
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