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3-Methyl-1H-indazole-6-carboxylic acid is a heterocyclic organic compound with the molecular formula C10H9NO2. It is a derivative of the indazole class, characterized by the presence of a methyl group and a carboxylic acid group at specific positions on the molecule. 3-Methyl-1H-indazole-6-carboxylic acid has garnered interest in the pharmaceutical industry and medicinal chemistry research due to its potential applications and biological activity.

201286-96-6

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201286-96-6 Usage

Uses

Used in Pharmaceutical Industry:
3-Methyl-1H-indazole-6-carboxylic acid is used as a key intermediate in the synthesis of novel drug candidates for various therapeutic applications. Its unique chemical structure allows for the development of new compounds with potential pharmacological effects.
Used in Medicinal Chemistry Research:
3-Methyl-1H-indazole-6-carboxylic acid serves as an important compound in medicinal chemistry research, where it is studied for its potential biological activity and pharmacological effects. This research aims to uncover its therapeutic potential and contribute to the discovery of new drugs for treating various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 201286-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,2,8 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 201286-96:
(8*2)+(7*0)+(6*1)+(5*2)+(4*8)+(3*6)+(2*9)+(1*6)=106
106 % 10 = 6
So 201286-96-6 is a valid CAS Registry Number.

201286-96-6SDS

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 3-methyl-2H-indazole-6-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-methyl-indazole-6-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:201286-96-6 SDS

201286-96-6Relevant academic research and scientific papers

SPIROKETONE ACETYL-COA CARBOXYLASE INHIBITORS

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, (2008/12/06)

The invention provides compounds of Formula (1) or a pharmaceutically acceptable salt of said compound, wherein R1, R2, R3, R4, R5, R6, R7, R8 and R9 are as described herein; pharmaceutical compositions thereof; and the use thereof in treating mammals suffering from the condition of being overweight.

Sulfonamide compounds and medicinal use thereof

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, (2010/02/04)

A sulfonamide compound of the formula (I):R 1 --SO 2 NHCO--A--R 2 (I)wherein R 1 is alkyl, alkenyl, alkynyl and the like; A is an optionally substituted heteropolycyclic group except benzimidazolyl, indolyl, 4,7-dihydrobenzimidazolyl and 2,3-dihydrobenzoxazinyl; X is alkylene, oxa, oxa(lower)alkylene and the like; and R 2 is optionally substituted aryl, substituted biphenylyl and the like, a salt thereof and a pharmaceutical composition comprising the same. The sulfonamide compound is effective for the diseases treatable based on their blood sugar level-depressing activity, cGMP-PDE (especially PDE-V)-inhibiting activity, smooth muscle relaxing activity, bronchodilating activity, vasodilating activity, smooth muscle cell suppressing activity, and antiallergic activity.

Substituted azabicyclic compounds

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, (2008/06/13)

This invention is directed to certain physiologically active compounds of formula (I) wherein represents a bicyclic ring system, of about 10 to about 13 ring members, in which the ring is an azaheterocycle, and the ring represents an azaheteroaryl ring, or an optionally halo substituted benzene ring; and N-oxides thereof, and their prodrugs, and pharmaceutically acceptable salts and solvates of the compounds of formula (I) and N-oxides thereof, and their prodrugs. Such compounds inhibit the production or physiological effects of TNF and inhibit cyclic AMP phosphodiesterase. The invention is also directed to pharmaceutical compositions comprising compounds of formula (I), their pharmaceutical use and methods for their preparation.

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