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Methyl 2-methyl-6-nitro-2H-indazole-3-carboxylate is a chemical compound with the molecular formula C10H9N3O4. It is a nitroaromatic compound with a methyl ester functional group and a carboxylate group, commonly used in the synthesis of pharmaceuticals and agrochemicals. This chemical has potential applications in the field of medicine, specifically in the development of anti-inflammatory and antimicrobial drugs. Its aromatic and nitro functional groups make it an important building block for the synthesis of various biologically active compounds. Additionally, it can be utilized as a reagent in organic synthesis and chemical research.

1058740-89-8

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1058740-89-8 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 2-methyl-6-nitro-2H-indazole-3-carboxylate is used as a building block for the synthesis of various biologically active compounds, specifically in the development of anti-inflammatory and antimicrobial drugs. Its aromatic and nitro functional groups contribute to the creation of novel drug candidates with potential therapeutic benefits.
Used in Agrochemical Industry:
Methyl 2-methyl-6-nitro-2H-indazole-3-carboxylate is used as a key intermediate in the synthesis of agrochemicals, particularly in the development of pesticides and herbicides. Its chemical properties allow for the creation of effective compounds that can protect crops and enhance agricultural productivity.
Used in Organic Synthesis:
Methyl 2-methyl-6-nitro-2H-indazole-3-carboxylate is used as a reagent in organic synthesis, enabling the formation of a wide range of chemical compounds. Its versatility in reactions makes it a valuable tool for chemists in the development of new materials and pharmaceuticals.
Used in Chemical Research:
Methyl 2-methyl-6-nitro-2H-indazole-3-carboxylate is used as a research compound in the study of chemical reactions and mechanisms. Its unique structure and functional groups provide insights into the behavior of nitroaromatic compounds and their potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1058740-89-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,8,7,4 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1058740-89:
(9*1)+(8*0)+(7*5)+(6*8)+(5*7)+(4*4)+(3*0)+(2*8)+(1*9)=168
168 % 10 = 8
So 1058740-89-8 is a valid CAS Registry Number.

1058740-89-8Relevant academic research and scientific papers

SUBSTITUTED ARYLSULFONYLAMINOMETHYLPHOSPHONIC ACID DERIVATIVES, THEIR PREPARATION AND THEIR USE IN THE TREATMENT OF TYPE I AND II DIABETES MELLITUS

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Page/Page column 66-67, (2009/03/07)

The present invention relates to substituted arylsulphonylaminomethylphosphonic acid derivatives of general formula (I) wherein R, X, Y and Z are defined as in claim 1, the tautomers, enantiomers, diastereomers, mixtures thereof and salts thereof which ha

NEW SUBSTITUTED ARYLSULPHONYLGLYCINES, THE PREPARATION THEREOF AND THE USE THEREOF AS PHARMACEUTICAL COMPOSITIONS

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Page/Page column 138-139, (2008/12/07)

The present invention relates to substituted arylsulphonylglycines of general formula (I) wherein R, X, Y and Z are defined as in claim 1, the tautomers, enantiomers, diastereomers, mixtures thereof and salts thereof, which have valuable pharmacological properties, particularly the suppression of the interaction of glycogen phosphorylase a with the GL subunit of glycogen-associated protein phosphatase 1 (PP1 ), and their use as pharmaceutical compositions.

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