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Ethyl 6-amino-1H-indazole-7-carboxylate is a heterocyclic chemical compound with the molecular formula C10H11N3O2. It features an indazole ring and an ethyl ester group, making it a significant compound in the fields of organic synthesis and pharmaceuticals. Known for its potential biological activities, including anti-inflammatory and anti-microbial properties, Ethyl 6-aMino-1H-indazole-7-carboxylate is also a promising candidate for the development of new pharmaceutical drugs for a variety of medical conditions.

73907-99-0

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73907-99-0 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 6-amino-1H-indazole-7-carboxylate is used as a key intermediate in organic synthesis for the production of potential drug candidates. Its unique structure and properties make it a valuable component in the creation of new medications.
Used in Organic Synthesis:
In the realm of organic synthesis, ethyl 6-amino-1H-indazole-7-carboxylate is utilized as a building block for the synthesis of various complex organic molecules, contributing to the development of novel chemical entities.
Used in Anti-inflammatory Applications:
Due to its anti-inflammatory properties, ethyl 6-amino-1H-indazole-7-carboxylate is studied for its potential use in the development of pharmaceuticals aimed at reducing inflammation and associated symptoms in various medical conditions.
Used in Anti-microbial Applications:
Its anti-microbial properties position ethyl 6-amino-1H-indazole-7-carboxylate as a candidate for the development of new antimicrobial agents, which could be crucial in combating drug-resistant infections.
Used in Drug Development for Medical Conditions:
Ethyl 6-amino-1H-indazole-7-carboxylate is explored for its potential in the development of pharmaceutical drugs to treat a range of medical conditions, highlighting its versatility and importance in medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 73907-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,0 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73907-99:
(7*7)+(6*3)+(5*9)+(4*0)+(3*7)+(2*9)+(1*9)=160
160 % 10 = 0
So 73907-99-0 is a valid CAS Registry Number.

73907-99-0Downstream Products

73907-99-0Relevant academic research and scientific papers

Synthesis of prox-Benzoisoallopurinol

Foster, Robert H.,Leonard, Nelson J.

, p. 3072 - 3077 (1980)

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.

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