73387-58-3

Usage

Chemical structure

1H-Pyrazole, 5-(4-methoxyphenyl)-1-methylis a heterocyclic compound with a pyrazole ring, containing a methyl group at the 1-position and a 4-methoxyphenyl group at the 5-position.

Derivative

It is a derivative of pyrazole with a 5-(4-methoxyphenyl)-1-methyl substituent.

Potential applications

1H-Pyrazole, 5-(4-methoxyphenyl)-1-methylhas potential applications in medicinal chemistry due to its pharmacological properties.

Pharmacological properties

The compound has been studied for its anti-inflammatory, analgesic, and antipyretic activities.

Further research

The specific properties and uses of 1H-Pyrazole, 5-(4-methoxyphenyl)-1-methylin various fields of chemistry and biochemistry would depend on further research and testing.

Upstream product

• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 18096-70-3 3-(dimethylamino)-1-(4-methoxyphenyl)prop-2-en-1-one 
• 930-36-9 1-methyl-1H-pyrazole 
• 104-92-7 1-bromo-4-methoxy-benzene 

Downstream Products

• 1206970-50-4 4-(1-methyl-1H-pyrazol-5-yl)phenol 

Relevant academic research and scientific papers

VASCULAR ADHESION PROTEIN-1 (VAP-1) MODULATORS AND THERAPEUTIC USES THEREOF

Disclosed herein are small molecule Vascular Adhesion Protein- 1 (VAP-1) modulator compositions, pharmaceutical compositions, the use and preparation thereof.

Mild palladium-catalyzed regioselective direct arylation of azoles promoted by tetrabutylammonium acetate

A mild, general, and convenient palladium-catalyzed direct arylation of the 5-position of azoles with aryl bromides, efficiently promoted by tetrabutylammonium acetate, is described. 1-Methylpyrazole, oxazole, and thiazole reacted at 70°C in N,N-dimethyla

Pd-catalysed direct 5-arylation of 1-methylpyrazole with aryl bromides

1-Methylpyrazole was found to be a suitable partner for palladium-catalysed direct arylation through C-H activation/functionalisation using aryl bromides. The reaction conditions and the nature of the catalyst were found to have a determining influence on

Thermolyses of 1,1-dimethyl-2-pyrazolinium fluoborates - Evidence for spiro--1-aza-1,4,6-octatrienyl cation

Thermolyses of 3-aryl-1,1-dimethyl-2-pyrazolinium fluoborates give an isomeric mixture of 3-aryl-1-methylpyrazole and 5-aryl-1-methylpyrazole as major products in complete contrast to the corresponding acyclic analogs. 2,6-Diaryl-3-methylpyridines were isolated only in trace quantities.The probable reasons for this unique behaviour was explored using semi-empirical calculations, non-kinetic methods and radiolabelling experiments.A pathway was proposed.