(3-(4-Fluorophenyl)isoxazol-5-yl)methanol

97%

  • Product Code: 85280
  CAS:    206055-89-2
Molecular Weight: 193.17 g./mol Molecular Formula: C₁₀H₈FNO₂
EC Number: MDL Number: MFCD06738489
Melting Point: Boiling Point: 358.46°C at 760 mmHg
Density: Storage Condition: Room temperature, dry and sealed
Product Description: This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting neurological disorders. Its structure, featuring a fluorophenyl group and an isoxazole ring, makes it valuable for developing molecules with potential anti-inflammatory, analgesic, or anticonvulsant properties. Researchers often explore its derivatives for their ability to modulate specific receptors or enzymes in the central nervous system. Additionally, it is employed in the development of novel therapeutic agents for conditions like epilepsy, chronic pain, and anxiety disorders. Its versatility in chemical modifications allows for the creation of diverse compounds with optimized pharmacological profiles.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $46.92
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0.250 10-20 days $69.74
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1.000 10-20 days $175.41
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5.000 10-20 days $527.92
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(3-(4-Fluorophenyl)isoxazol-5-yl)methanol
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting neurological disorders. Its structure, featuring a fluorophenyl group and an isoxazole ring, makes it valuable for developing molecules with potential anti-inflammatory, analgesic, or anticonvulsant properties. Researchers often explore its derivatives for their ability to modulate specific receptors or enzymes in the central nervous system. Additionally, it is employed in the development of novel therapeutic agents for conditions like epilepsy, chronic pain, and anxiety disorders. Its versatility in chemical modifications allows for the creation of diverse compounds with optimized pharmacological profiles.
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