Pyrazolo[1,5-a]pyridine-7-carbaldehyde

97%

  • Product Code: 126318
  CAS:    362661-83-4
Molecular Weight: 146.15 g./mol Molecular Formula: C8H6N2O
EC Number: MDL Number: MFCD06739029
Melting Point: 83 - 88 ℃ Boiling Point:
Density: 1.24±0.1 g/cm3(Predicted) Storage Condition: room temperature
Product Description: Pyrazolo[1,5-a]pyridine-7-carbaldehyde is widely utilized in pharmaceutical research and development as a key intermediate in the synthesis of various bioactive compounds. Its structure is particularly valuable in the creation of molecules with potential therapeutic applications, such as anticancer, antiviral, and anti-inflammatory agents. The aldehyde functional group in this compound allows for versatile chemical modifications, enabling the formation of Schiff bases, hydrazones, and other derivatives that can be screened for biological activity. Additionally, it is employed in the design of heterocyclic compounds for use in medicinal chemistry, where it contributes to the development of novel drugs targeting specific enzymes or receptors. Its role in organic synthesis also extends to the production of fluorescent probes and materials for optoelectronic applications.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days Ft21,548.22
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Pyrazolo[1,5-a]pyridine-7-carbaldehyde
Pyrazolo[1,5-a]pyridine-7-carbaldehyde is widely utilized in pharmaceutical research and development as a key intermediate in the synthesis of various bioactive compounds. Its structure is particularly valuable in the creation of molecules with potential therapeutic applications, such as anticancer, antiviral, and anti-inflammatory agents. The aldehyde functional group in this compound allows for versatile chemical modifications, enabling the formation of Schiff bases, hydrazones, and other derivatives that can be screened for biological activity. Additionally, it is employed in the design of heterocyclic compounds for use in medicinal chemistry, where it contributes to the development of novel drugs targeting specific enzymes or receptors. Its role in organic synthesis also extends to the production of fluorescent probes and materials for optoelectronic applications.
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