73907-98-9

Basic information

• Product Name: Methyl 6-aMino-1H-indazole-7-carboxylate
• Synonyms: Methyl 6-aMino-1H-indazole-7-carboxylate
• CAS NO: 73907-98-9
• Molecular Formula: C9H9N3O2
• Molecular Weight: 191.18666
• Mol File: 73907-98-9.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• CAS DataBase Reference: Methyl 6-aMino-1H-indazole-7-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 6-aMino-1H-indazole-7-carboxylate(73907-98-9)
• EPA Substance Registry System: Methyl 6-aMino-1H-indazole-7-carboxylate(73907-98-9)

Safety Data

• Hazardous Substances Data: 73907-98-9(Hazardous Substances Data)

Usage

General Description

Methyl 6-amino-1H-indazole-7-carboxylate is a chemical compound with the molecular formula C9H8N4O2. It is commonly used in the pharmaceutical and chemical research industries as a building block for the synthesis of various organic compounds. Methyl 6-aMino-1H-indazole-7-carboxylate is a derivative of indazole, a heterocyclic aromatic organic compound with applications in medical and agricultural fields. Methyl 6-amino-1H-indazole-7-carboxylate has been studied for its potential medicinal properties, including anti-inflammatory and analgesic effects. It is also a promising candidate for the development of new drugs for the treatment of various diseases. Overall, this compound plays a significant role in the advancement of pharmaceutical and chemical research.

Upstream product

• 6967-12-0 6-amino-1H-indazole 
• 186581-53-3 diazomethane 
• 73907-95-6 6-aminoindazole-7-carboxylic acid 
• 73907-93-4 6-(isonitrosoacetamido)indazole 
• 73907-93-4 2-[(E)-Hydroxyimino]-N-(1H-indazol-6-yl)-acetamide 
• 77929-34-1 6-(hydroximinoacetyl)-amino-1H-indazole hydrochloride 
• 73907-94-5 pyrrolo<2,3-g>indazole-7,8-dione 

Downstream Products

• 73907-90-1 prox-benzoisoallopurinol 
• 154597-37-2 6-amino-7-indazolecarboxaldehyde 

Relevant articles and documents

PESTICIDES CONTAINING A BICYCLIC BISAMIDE STRUCTURE

Compounds of formula (I), wherein the substituents are as defined in claim 1, and the agrochemically acceptable salts and all stereoisomers and tautomeric forms of the compounds of formula I can be used as agrochemical active ingredients and can be prepared in a manner known per se.

SYNTHESIS OF A -LINKED PYRAZOLOQUINAZOLINONE

A convenient synthesis is described for pyrazoloquinazolin-9-one (4), an internally expanded benzolog of the biologically relevant pyrazolopyrimidines (2).

Synthesis of prox-Benzoisoallopurinol

Pyrazoloquinazolin-9-one (prox-benzoisoallopurinol, 1), an extented analogue of 7-hydroxypyrazolopyrimidine (isoallopurinol, 2) and a potential dimensional probe for substrates of xanthine oxidase, has been synthesized by two independent routes.The title compound, prepared by elaboration of either a suitably substituted indazole or a quinazolinone, was found to be an active substrate for and an alternative-substrate inhibitor of xanthine oxidase.The product of enzymatic oxidation of prox-benzoisoallopurinol has been identified as the corresponding prox-benzoisoalloxanthine.