1H-Indazol-3-ylacetic acid, with the CAS number 26663-42-3, is an organic compound characterized by its indazole core, which is a bicyclic structure containing a five-membered ring fused to a six-membered ring. This compound features an acetic acid functional group attached to the indazole at the 3-position, contributing to its acidic properties. It is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, reflecting its ability to form hydrogen bonds due to the presence of the carboxylic acid group. The compound may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of new therapeutic agents. Its molecular structure allows for potential interactions with various biological targets, and it may participate in various chemical reactions typical of carboxylic acids and heterocyclic compounds. As with many organic compounds, handling should be done with care, considering safety data and potential hazards associated with its use.

1H-indazol-3-ylacetic acid

(1H-INDAZOL-3-YL)-ACETIC ACID

2-(1H-Indazol-3-yl)acetic acid

(1H-INDAZOL-3-YL)-ACETIC ACID is a reactive ligand that has been shown to bind to aryloxyalkyl groups, water molecules, and aminoacetic esters. In vivo studies have shown that this compound can be used to esterify carboxylate anions. The crystal x-ray diffraction of the (1H-INDAZOL-3-YL)-ACETIC ACID molecule has revealed bidentate binding. This compound has been shown to inhibit bacterial growth by disrupting their cell membranes and respiratory diseases by inhibiting enzymes that are involved in the synthesis of rhodopsin.

CAS 26663-42-3: 1H-indazol-3-ylacetic acid

(1H-INDAZOL-3-YL)-ACETIC ACID

Ref: 10-F793893

2-(1H-Indazol-3-yl)acetic acid

Ref: 10-F224628

(1H-INDAZOL-3-YL)-ACETIC ACID

Ref: 3D-FI156617

2-(1H-Indazol-3-yl)acetic acid

Ref: IN-DA0037PJ

2-(1H-Indazol-3-yl)acetic acid

Ref: 54-OR76197