1848-41-5

Usage

Uses

Used in Organic Chemistry:
3-methoxy-1H-indazole is used as a precursor in the synthesis of various pharmaceuticals and other organic compounds, leveraging its unique molecular structure to facilitate the creation of diverse chemical entities.
Used in Pharmaceutical Research:
In the field of pharmaceutical research, 3-methoxy-1H-indazole is utilized for its potential as a psychedelic drug, with ongoing studies investigating its effects on the central nervous system. Its precise pharmacological and toxicological properties, while not fully elucidated, make it a subject of interest for further exploration and development in medicinal applications.

Upstream product

• 62723-78-8 2-methoxymethylaniline 
• 7364-25-2 1H-indazol-3-ol 
• 91087-91-1 1-N-ethoxycarbonyl-3-methoxy-1H-indazole 
• 16105-24-1 1-N-ethoxycarbonyl-3-hydroxy-1H-indazole 
• 74-88-4 methyl iodide 
• 5575-35-9 1-acetyl-3-methylindazole 

Relevant academic research and scientific papers

SELECTIVE INHIBITORS OF CLINICALLY IMPORTANT MUTANTS OF THE EGFR TYROSINE KINASE

The present invention provides compounds of Formula (I) or a subgeneric structure or species thereof, or a pharmaceutically acceptable salt, ester, solvate, and/or prodrug thereof, and methods and compositions for treating or ameliorating abnormal cell pr

Synthesis, biological evaluation and chemometric analysis of indazole derivatives. 1,2-Disubstituted 5-nitroindazolinones, new prototypes of antichagasic drug

Chagas disease chemotherapy, currently based on only two drugs, nifurtimox and benznidazole, is far from satisfactory and therefore the development of new antichagasic compounds remains an important goal. On the basis of antichagasic properties previously

Aromatic Diazonium Salts, X. - A One-Pot Procedure for the Jacobson Synthesis of Indazole

Procedures are described for a one-pot synthesis of 1H-indazole and substituted indazoles 3 in good yield (Table 1) from o-toluidines 2, alkyl nitrite or nitrous oxides, potassium acetate, and acetic anhydride in benzene.The spectroscopic properties of substituted indazoles (Tables 2-4) are discussed. - 4-Phenylcinnoline (18) is prepared by the same procedure from o-(α-methylenebenzyl)aniline.