3198-98-9

Usage

Structure

1H-Pyrazole-3,4-dicarboxylic acid, 1-phenyl-, dimethyl ester

Type of compound

Ester

Parent compound

1-phenyl-1H-pyrazole-3,4-dicarboxylic acid

Uses

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Properties

Insecticidal and fungicidal

Applications

Agricultural industry and potential treatment of various diseases

Safety precautions

Handle with care and ensure safety measures are in place in laboratory or industrial settings.

Upstream product

• 922-67-8 propynoic acid methyl ester 
• 58131-64-9 methyl 2-chloro-2-(2-phenylhydrazono)acetate 
• 2055-52-9 methyl 1-phenyl-1H-1,2,3-triazole-4-carboxylate 
• 762-42-5 dimethyl acetylenedicarboxylate 
• 13148-78-2 1,4-diphenyl-[1,2,3]-triazole 
• 34296-51-0 1-phenyl-1,2,3-triazole-4-carbaldehyde 
• 1453-81-2 1-phenyl-1,2,3-triazole 
• 508191-77-3 3-phenylsydnone 

Downstream Products

• 892962-79-7 1-(phenyl)-1H-pyrazol-3,4-dicarbohydrazide 
• 3198-97-8 1-phenyl-1H-pyrazole-3,4-dicarboxylic acid 
• 23245-12-7 2-phenyl-5,6-dihydro-2H-pyrazolo[3,4-d]pyridazine-4,7-dione 
• 892962-85-5 1-phenyl-N₃',N₄'-dibenzoyl-1H-pyrazole-3,4-dicarbohydrazide 

Relevant academic research and scientific papers

Recyclable supported catalysts in microwave-assisted reactions: first Diels-Alder cycloaddition of a triazole ring

We describe here the first example in which a 1,2,3-triazole ring acts as a diene towards DMAD in microwave-assisted solvent-free Diels-Alder cycloadditions. The extrusion of a molecule of a nitrile affords pyrazole derivatives as the products. The yields

Novel pyrazole derivatives via ring transformations: Anti-inflammatory and antifungal activity studies

In this paper, the synthesis of novel pyrazoles and their in vitro anti-inflammatory and in-vitro antifungal assay have been reported. These compounds were docked into the inducible nitric oxide synthase (iNOS) oxygenase dimer. The compounds 3c, 7a, 7c, 8

Solvent-free synthesis of bis-hydrazones through 1,3-dipolar cycloaddition of sydnone and study of their optical, molecular docking, and antioxidant properties

A series of new 1-(aryl)-1H-pyrazol-3,4-bis (aryl)-3,4-dicarbohydrazones (4) was obtained by the condensation of 1-arylpyrazole-3,4-dicarbohydrazides (3) with various aryl aldehydes under solvent-free conditions. The structures of the newly synthesized hy

Synthesis and characterization of soluble conjugated poly(p- phenylenevinylene) derivatives constituted of alternating pyrazole and 1,3,4-oxadiazole moieties

New soluble poly(p-phenylenevinylene) derivatives with 1,3,4-oxadiazole and pyrazole rings along the main chain were synthesized by Heck coupling. The new conjugated polymers are soluble in common organic solvents as a result of the fully conjugated backb

Synthesis, optical properties, and characterization of new soluble conjugated poly(p-phenylenevinylene) derivatives constituted of alternating pyrazole and 1,3,4-oxadiazole moieties

Two new soluble poly(p-phenylenevinylene) derivatives with 1,3,4-oxadiazole and pyrazole rings along the main core were successfully synthesized by 1,3-dipolar addition, dehydration, and Heck coupling reaction. The new conjugated polymers are soluble in c

New efficient blue-greenish electroluminescent materials of 1,3,4-oxadiazole-based pyrazole derivatives

Novel blue-greenish electroluminescent materials of 1,3,4-oxadiazole-based pyrazole derivatives as electronic-transporting molecules have been synthesized and characterized. Those compounds are convenient successful inducted a pyrazole chromophore and mul