1041481-59-7

Basic information

• Product Name: 4-Fluoro-1H-indazole-5-carboxylic acid
• Synonyms: 4-Fluoro-1H-indazole-5-carboxylic acid;5-Carboxy-4-fluoro-1H-indazole;4-Fluoro-1H-indazol-5-carboxylic acid;1H-indazole-5-carboxylic acid, 4-fluoro-
• CAS NO: 1041481-59-7
• Molecular Formula: C8H5FN2O2
• Molecular Weight: 180.1359032
• Mol File: 1041481-59-7.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Density: 1.610
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-Fluoro-1H-indazole-5-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Fluoro-1H-indazole-5-carboxylic acid(1041481-59-7)
• EPA Substance Registry System: 4-Fluoro-1H-indazole-5-carboxylic acid(1041481-59-7)

Safety Data

• Hazardous Substances Data: 1041481-59-7(Hazardous Substances Data)

Usage

General Description

4-Fluoro-1H-indazole-5-carboxylic acid is a chemical compound with the molecular formula C8H5FN2O2. It belongs to the class of organic compounds known as indazoles, which are aromatic heterocyclic compounds containing a pyrazole ring fused to a benzene ring. The 4-Fluoro-1H-indazole-5-carboxylic acid compound carries a fluorine atom at the 4th position and a carboxylic acid at the 5th position in the indazole ring. 4-Fluoro-1H-indazole-5-carboxylic acid is known for its reactivity and is often used in chemical synthesis. However, information regarding its specific applications, toxicological effects, and risk and safety assessments appear to be limited.

Upstream product

• 473416-81-8 4-fluoro-1H-indazole-5-carbonitrile 

Downstream Products

• 1041481-61-1 C₁₇H₁₆FN₅O₂S 
• 473416-82-9 4-fluoro-1H-indazole-5-carboxylic acid methyl ester 

Relevant articles and documents

PYRAZOLE COMPOUND AND MEDICINAL COMPOSITION CONTAINING THE SAME

The present invention provides a novel compound having an excellent JNK inhibitory effect. That is, it provides a compound represented by the following formula, a salt thereof or a hydrate of them. Wherein R1 designates -(CO)h-(NRa)j-(CRb=CRc)k-Ar (wherein Ra, Rb and Rc each independently designate a hydrogen atom, a halogen atom, hydroxyl group, an optionally substituted C1-6 alkyl group or the like; Cy designates a 5- or 6-membered heteroaryl; and V each independently designate the formula -L-X-Y (wherein L designates a single bond, an optionally substituted C1-6 alkylene group or the like; X designates a single bond or the formula -A- (wherein A designates NR2, O, CO, S, SO or SO2) and so on; and Y designates a hydrogen atom, a halogen atom, nitro group or the like).