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6-Nitro-3-indazolecarboxylic acid is a chemical compound that belongs to the class of organic compounds known as indazoles. It is a nitro derivative of indazolecarboxylic acid, featuring a nitro group at the 6-position and a carboxylic acid group at the 3-position of the indazole ring. This versatile compound is characterized by its molecular structure and properties, making it a promising candidate for use in various organic reactions and chemical synthesis.

857801-97-9

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857801-97-9 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
6-Nitro-3-indazolecarboxylic acid is used as a building block in the synthesis of various pharmaceuticals and agrochemicals. Its unique molecular structure and properties allow it to be incorporated into the development of new drugs and chemical compounds, contributing to the advancement of these industries.
Used in Medicinal Chemistry Research:
6-Nitro-3-indazolecarboxylic acid has shown potential biological activity in certain studies, making it an interesting target for medicinal chemistry research. Researchers can explore its potential applications in the development of new therapeutic agents and treatments for various diseases and conditions.
Used in Organic Reactions and Chemical Synthesis:
Due to its versatile molecular structure and properties, 6-Nitro-3-indazolecarboxylic acid is used in various organic reactions and chemical synthesis processes. It can be employed as a reactant or intermediate in the production of other chemical compounds, further expanding its applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 857801-97-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,8,0 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 857801-97:
(8*8)+(7*5)+(6*7)+(5*8)+(4*0)+(3*1)+(2*9)+(1*7)=209
209 % 10 = 9
So 857801-97-9 is a valid CAS Registry Number.

857801-97-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-nitro-1H-indazole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-nitroindazole-3-carboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:857801-97-9 SDS

857801-97-9Relevant academic research and scientific papers

Indoles, 1h-indazoles, 1,2-benzisoxazoles, 1,2-benzoisothiazoles, and preparation and uses thereof

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Page/Page column 38, (2008/06/13)

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nACh receptors), activation of nACh receptors, and the treatment of disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds (indazoles and benzothiazoles), which act as ligands for the α7 nACh receptor subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

INDOLES, 1H-INDAZOLES, 1,2-BENZISOXAZOLES, AND 1,2-BENZISOTHIAZOLES, AND PREPARATION AND USES THEREOF

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Page/Page column 37, (2008/06/13)

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nAChR), activation of nAChRs, and the treatment of disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds for example, indoles, 1H-indazoles, 1,2-benzisoxazoles, and 1,2-benzisothiazoles, which act as ligands for the α7 nAChR subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

1H-INDAZOLES, BENZOTHIAZOLES, 1,2-BENZOISOXAZOLES, 1,2-BENZOISOTHIAZOLES, AND CHROMONES AND PREPARATION AND USES THEREOF

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Page/Page column 69-70, (2008/06/13)

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nAChR), activation of nAChRs, and the treatment of disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds (indazoles and benzothiazoles), which act as ligands for the α7 nAChR subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

INDAZOLES, BENZOTHIAZOLES, BENZOISOTHIAZOLES, BENZISOXAZOLES, AND PREPARATION AND USES THEREOF

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Page/Page column 79-80, (2010/02/14)

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nACh receptors), activation of nACh receptors, and the treatment of disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds (e.g., indazoles and benzothiazoles), which act as ligands for the α7 nACh receptor subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

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