59843-49-1

Basic information

• Product Name: 3-(2-Methylphenyl)-1H-pyrazole
• Synonyms: 3-(2-Methylphenyl)-1H-pyrazole;3-O-TOLYL-1H-PYRAZOLE;3-(o-Tolyl)-1H-pyrazole, 2-(1H-Pyrazol-3-yl)toluene;5-(2-methylphenyl)-1H-pyrazole
• CAS NO: 59843-49-1
• Molecular Formula: C₁₀H₁₀N₂
• Molecular Weight: 158.1998
• Mol File: 59843-49-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-(2-Methylphenyl)-1H-pyrazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-Methylphenyl)-1H-pyrazole(59843-49-1)
• EPA Substance Registry System: 3-(2-Methylphenyl)-1H-pyrazole(59843-49-1)

Safety Data

• Hazardous Substances Data: 59843-49-1(Hazardous Substances Data)

Usage

General Description

3-(2-Methylphenyl)-1H-pyrazole is a chemical compound with the molecular formula C11H10N2. It is part of the pyrazole class of organic compounds and contains a pyrazole ring with a 2-methylphenyl group attached at the 3-position. 3-(2-Methylphenyl)-1H-pyrazole is used in scientific research and is known for its potential pharmacological properties, particularly as a potential inhibitor of certain enzymes. Its chemical structure and properties make it of interest for drug development and medicinal chemistry studies.

Upstream product

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Downstream Products

• 59843-50-4 N,N-dimethyl-2-(3-o-tolyl-pyrazol-1-yl)-propionamide 
• 59843-51-5 N,N-dimethyl-2-(5-o-tolyl-pyrazol-1-yl)-propionamide 
• 59844-45-0 2,N,N-trimethyl-2-(3-o-tolyl-pyrazol-1-yl)-propionamide 
• 59844-08-5 N,N-dimethyl-2-(3-o-tolyl-pyrazol-1-yl)-butyramide 
• 1335210-51-9 C₂₄H₁₈N₂ 

Relevant articles and documents

ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES

A compound having a structure of the formula Ir(LA)(LB), in which LA is a bidentate, tridentate, tetradentate, pentadentate, or hexadentate ligand and LB is a monodentate, bidentate, tridentate, or tetradentate ligand, or not present, and where the total denticity of LA plus LB is 6, and LA includes at least one structure of Formula I: is disclosed as a useful phosphorescent emitter compound.

A novel one-pot method for the preparation of pyrazoles by 1,3-dipolar cycloadditions of diazo compounds generated in situ

A convenient one-pot procedure for the preparation of pyrazoles by 1,3-dipolar cycloaddition of diazo compounds generated in situ has been developed. Diazo compounds derived from aldehydes were reacted with terminal alkynes to furnish regioselectively 3,5-disubstituted pyrazoles. Furthermore, the reaction of N-vinylimidazole and diazo compounds derived from aldehydes gave exclusively 3-substituted pyrazoles in a one-pot process.