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1058740-77-4

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1058740-77-4 Usage

Nitro derivative of indazole-3-carboxylic acid

This compound is derived from indazole-3-carboxylic acid by the addition of a nitro group, which influences its chemical properties and reactivity.

Methyl group at the 1 position

A methyl group (CH3) is attached to the indazole ring at the first position, contributing to the compound's structure and properties.

Nitro group at the 6 position

A nitro group (-NO2) is attached to the indazole ring at the sixth position, further affecting the compound's reactivity and properties.

Organic synthesis and pharmaceutical research

1-methyl-6-nitro-1H-indazole-3-carboxylic acid is commonly used as a building block for the synthesis of various biologically active compounds, making it a valuable component in creating new molecules.

Potential pharmacological properties

The compound has been studied for its possible anti-inflammatory and anticancer activities, indicating its potential as a therapeutic agent.

Medicinal chemistry tool

Due to its structure and reactivity, 1-methyl-6-nitro-1H-indazole-3-carboxylic acid is a valuable tool in medicinal chemistry for the development of new drug candidates.

Check Digit Verification of cas no

The CAS Registry Mumber 1058740-77-4 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, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1058740-77:
(9*1)+(8*0)+(7*5)+(6*8)+(5*7)+(4*4)+(3*0)+(2*7)+(1*7)=164
164 % 10 = 4
So 1058740-77-4 is a valid CAS Registry Number.

1058740-77-4Downstream Products

1058740-77-4Relevant articles and documents

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 65-66, (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

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