CAS 25627-89-8
:Pyrazolo[1,5-a]pyridine-3-carbonitrile
Description:
Pyrazolo[1,5-a]pyridine-3-carbonitrile is a heterocyclic organic compound characterized by its unique bicyclic structure, which consists of a pyrazole ring fused to a pyridine ring. This compound features a cyano group (-C≡N) at the 3-position of the pyrazolo ring, contributing to its reactivity and potential applications in various chemical reactions. It is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. The presence of both nitrogen atoms in the rings enhances its basicity and can influence its interaction with biological targets, making it of interest in medicinal chemistry. Pyrazolo[1,5-a]pyridine derivatives have been studied for their potential pharmacological properties, including anti-inflammatory and anticancer activities. The compound's molecular structure allows for various substitutions, which can further modify its chemical properties and biological activity. As with many heterocycles, it may also participate in coordination chemistry, forming complexes with metal ions. Safety data should be consulted for handling and usage, as with any chemical substance.
Formula:C8H5N3
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Found 4 products.
Pyrazolo[1,5-a]pyridine-3-carbonitrile
CAS:Pyrazolo[1,5-a]pyridine-3-carbonitrilePurity:98%Molecular weight:143.15g/molRef: 10-F639590
1g481.00€5g1,278.00€10g2,339.00€2.5g803.00€50mg127.00€100mg183.00€250mg260.00€500mg377.00€Pyrazolo[1,5-a]pyridine-3-carbonitrile
CAS:Pyrazolo[1,5-a]pyridine-3-carbonitrile is a crystalline solid in the form of an amorphous or polymorph. It has been shown to inhibit the kinase activity of protein tyrosine phosphatases and may be useful for the treatment of gastrointestinal disorders. The compound has also been shown to have antioxidant properties, which may be related to its ability to inhibit oxidative phosphorylation by inhibiting the mitochondrial membrane potential. Pyrazolo[1,5-a]pyridine-3-carbonitrile has also been shown to suppress proliferation and induce apoptosis in some types of cancer cells. This compound can serve as a nitrogen source for microbial growth and can inhibit bacterial growth by acting as an inhibitor of indolizine synthesis or nitrogen fixation.Formula:C8H5N3Purity:Min. 95%Molecular weight:143.15 g/mol




