CAS 90004-04-9
:1H-Indazole-3-carboxamide
Description:
1H-Indazole-3-carboxamide, with the CAS number 90004-04-9, is a chemical compound characterized by its indazole core, which is a five-membered aromatic ring containing two nitrogen atoms. This compound features a carboxamide functional group (-C(=O)NH2) at the 3-position of the indazole ring, contributing to its potential biological activity. It is typically a white to off-white solid and is soluble in polar organic solvents. The presence of the carboxamide group suggests that it may participate in hydrogen bonding, influencing its solubility and reactivity. 1H-Indazole-3-carboxamide has garnered interest in medicinal chemistry due to its potential pharmacological properties, including anti-inflammatory and anticancer activities. Its structure allows for various modifications, which can enhance its biological efficacy or selectivity. As with many indazole derivatives, the compound's properties can be influenced by substituents on the indazole ring, making it a versatile scaffold for drug development. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.
Formula:C8H7N3O
Synonyms:- 1H-Indazole-3-carboxamide(6CI,7CI,9CI)
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Found 5 products.
1H-Indazole-3-carboxamide
CAS:Formula:C8H7N3OPurity:98%Color and Shape:SolidMolecular weight:161.16071H-Indazole-3-carboxamide
CAS:Controlled Product<p>1H-Indazole-3-carboxamide is a nitro, quinoline derivative that is used as a research tool for the study of cancer. It has been shown to have a pharmacokinetic profile similar to that of indazole carboxamide, which is a synthetic cannabinoid. 1H-Indazole-3-carboxamide has been shown to inhibit kinase activity selectively and has been found in human liver samples. This compound can be synthesized by combining hydrochloric acid with an amide and an indazole carboxylic acid.</p>Formula:C8H7N3OPurity:Min. 95%Molecular weight:161.16 g/mol
