42329-05-5

Basic information

• Product Name: 3,5-Dimethyl-1-(4-pyridinylcarbonyl)-1H-pyrazole
• Synonyms: 3,5-Dimethyl-1-(4-pyridinylcarbonyl)-1H-pyrazole;4-[(3,5-dimethyl-1H-pyrazol-1-yl)carbonyl]pyridine
• CAS NO: 42329-05-5
• Molecular Formula: C11H11N3O
• Molecular Weight: 201.2245
• Mol File: 42329-05-5.mol
• Article Data: 7

Chemical Properties

• Melting Point: 172 °C
• Boiling Point: 375.6°Cat760mmHg
• Flash Point: 181°C
• Appearance: /
• Density: 1.19g/cm³
• Vapor Pressure: 7.69E-06mmHg at 25°C
• Refractive Index: 1.613
• PKA: 1.97±0.10(Predicted)
• CAS DataBase Reference: 3,5-Dimethyl-1-(4-pyridinylcarbonyl)-1H-pyrazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Dimethyl-1-(4-pyridinylcarbonyl)-1H-pyrazole(42329-05-5)
• EPA Substance Registry System: 3,5-Dimethyl-1-(4-pyridinylcarbonyl)-1H-pyrazole(42329-05-5)

Safety Data

• Hazardous Substances Data: 42329-05-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H11N3O/c1-8-7-9(2)14(13-8)11(15)10-3-5-12-6-4-10/h3-7H,1-2H3

Upstream product

• 54-85-3 isoniazid 
• 123-54-6 acetylacetone 
• 67-51-6 3,5-dimethyl-1H-pyrazole 
• 39178-35-3 isonicotinoyl chloride hydrochloride 

Relevant articles and documents

Synthesis of quinoxaline, benzimidazole and pyrazole derivatives under the catalytic influence?of biosurfactant-stabilized iron nanoparticles in water

Abstract: We have reported the synthesis, characterization, and catalytic applications of amorphous iron nanoparticles (FeNPs) using aqueous leaves extract of renewable natural resource Boswellia serrata plant. Synthesized FeNPs were stabilized in situ by the addition of aqueous pod extracts of Acacia concinna as a biosurfactant (pH 3.11). The structural investigation of biosynthesized nanoparticles was performed using UV–visible spectroscopy, X-ray diffraction analysis, selected area electron diffraction, energy-dispersive X-ray spectroscopy, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, thermogravimetric analysis, and BET analysis. The FeNPs were amorphous in nature with average particle size ~ 19?nm and successfully employed as heterogeneous catalyst for the synthesis of quinoxaline, benzimidazole, and pyrazole derivatives in aqueous medium at ambient conditions. The FeNPs could be recycled up to five times with modest change in the catalytic activity. Graphic abstract: [Figure not available: see fulltext.].

An efficient practical chemo-enzymatic protocol for the synthesis of pyrazoles in aqueous medium at ambient temperature

An expeditious oxidative cyclocondensation reaction of hydrazines/hydrazides with 1,3-dicarbonyl compound was efficiently developed in aqueous medium using Saccharomyces cerevisae (baker's yeast) as a whole cell biocatalyst at room temperature. The method has been assigned using green chemistry measures and found to give a range of N-substituted pyrazoles with moderate to excellent yields (70-92%). The reaction progress was monitored by gas chromatography.

Hydrotrope: Green and rapid approach for the catalyst-free synthesis of pyrazole derivatives

An efficient synthesis of pyrazole derivatives by condensation of 1,3-diketone and hydrazines/hydrazides has been achieved in aqueous hydrotropic solution under catalyst-free conditions within a very short time. The present protocol is beneficial as it includes mild reaction conditions, shorter reaction times, use of universal solvent water, which avoids volatile organic solvents, high yields of products, and being environmentally friendly.