317806-51-2

Basic information

• Product Name: 1H-Pyrazole-4-carboxylicacid,5-amino-1-methyl-3-(trifluoromethyl)-(9CI)
• Synonyms: 1H-Pyrazole-4-carboxylicacid,5-amino-1-methyl-3-(trifluoromethyl)-(9CI);5-Amino-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid;5-aMino-3-(trifluoroMethyl)-1-Methyl-1H-pyrazole-4-carboxylic acid;1H-Pyrazole-4-carboxylicacid,5-aMino-1-Methyl-3-(trifluoroMethyl)
• CAS NO: 317806-51-2
• Molecular Formula: C6H6F3N3O2
• Molecular Weight: 209.126
• Product Categories: AMINOACID;Building Blocks;Pyrazole
• Mol File: 317806-51-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 340.6±42.0 °C(Predicted)
• Appearance: /
• Density: 1.73±0.1 g/cm3(Predicted)
• PKA: 3.67±0.36(Predicted)
• CAS DataBase Reference: 1H-Pyrazole-4-carboxylicacid,5-amino-1-methyl-3-(trifluoromethyl)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrazole-4-carboxylicacid,5-amino-1-methyl-3-(trifluoromethyl)-(9CI)(317806-51-2)
• EPA Substance Registry System: 1H-Pyrazole-4-carboxylicacid,5-amino-1-methyl-3-(trifluoromethyl)-(9CI)(317806-51-2)

Safety Data

• Hazardous Substances Data: 317806-51-2(Hazardous Substances Data)

Usage

General Description

"1H-Pyrazole-4-carboxylic acid, 5-amino-1-methyl-3-(trifluoromethyl)-(9CI)" is a specific chemical compound with complex molecular structure. It contains several functional groups that contribute to its properties, including a pyrazole ring, a carboxylic acid group, an amino group, a methyl group and a trifluoromethyl group. The compound's 1-methyl and 3-trifluoromethyl substitutions on the pyrazole ring along with 5-amino-1-methyl functional group contribute to its overall stability and reactivity. Due to its structure, this compound may be used or studied in the field of pharmaceuticals or specialty chemical synthesis, though it is topic-specific and may require further research. Further information such as its precise molecular formula, weight, and its other physical and chemical properties are important parameters to understand the chemical thoroughly.

Upstream product

• 317806-48-7 ethyl 5-amino-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylate 

Relevant articles and documents

SUBSTITUTED BICYCLIC HETEROCYCLIC COMPOUNDS AS NADPH OXIDASE INHIBITORS

The present application relates to substituted fused heteroaryl and heterocyclic compounds, useful as nicotinamide adenine dinucleotide phosphate oxidase inhibitors (NADPH oxidase inhibitors), processes for their preparation, pharmaceutical compositions comprising the compounds, and the use of the compounds or the compositions in the treatment or prevention of various diseases, conditions and/or disorders mediated by NADPH oxidase. (Formula I)

5-aminopyrazole-4-carboxylate derivative and process for preparing the same

A 5-aminopyrazole-4-carboxylate derivative represented by the formula (1) is prepared by reacting a compound represented by the formula (2) with a hydrazine compound represented by the formula (3) or hydrate, hydrochloride, hydrobromide or sulfate of the same according to the reaction formula (C): wherein R1is a straight or branched C1 to C4 alkyl group which can be substituted with a halogen atom, R2is a hydrogen atom, straight or branched C1 to C4 alkyl group or an unsubstituted or substituted phenyl group, and R3is a straight or branched C1 to C4 alkyl group, and M is an alkali metal. The 5-aminopyrazole-4-carboxylate derivative obtained by the preparation process of the invention is useful for an intermediate of agricultural chemicals and medicines, fungicides in particular.