Ethyl 4-bromo-6-fluoropyrazolo[1,5-a]pyridine-3-carboxylate

95%

  • Product Code: 47508
  CAS:    2177264-85-4
Molecular Weight: 287.0851 g./mol Molecular Formula: C₁₀H₈BrFN₂O₂
EC Number: MDL Number: MFCD31652659
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: Ethyl 4-bromo-6-fluoropyrazolo[1,5-a]pyridine-3-carboxylate is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active compounds. Its structure, featuring both bromo and fluoro substituents, makes it a versatile building block for designing molecules with potential therapeutic applications. Researchers often employ it in the creation of drug candidates targeting various diseases, including cancer, inflammation, and neurological disorders. Additionally, its pyrazolo[1,5-a]pyridine core is valuable in medicinal chemistry for optimizing drug properties such as potency, selectivity, and bioavailability. The compound is also used in academic and industrial laboratories to explore new chemical reactions and develop innovative synthetic methodologies.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿6,030.00
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Ethyl 4-bromo-6-fluoropyrazolo[1,5-a]pyridine-3-carboxylate
Ethyl 4-bromo-6-fluoropyrazolo[1,5-a]pyridine-3-carboxylate is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active compounds. Its structure, featuring both bromo and fluoro substituents, makes it a versatile building block for designing molecules with potential therapeutic applications. Researchers often employ it in the creation of drug candidates targeting various diseases, including cancer, inflammation, and neurological disorders. Additionally, its pyrazolo[1,5-a]pyridine core is valuable in medicinal chemistry for optimizing drug properties such as potency, selectivity, and bioavailability. The compound is also used in academic and industrial laboratories to explore new chemical reactions and develop innovative synthetic methodologies.
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