3198-98-9

Basic information

• Product Name: 1H-Pyrazole-3,4-dicarboxylic acid, 1-phenyl-, dimethyl ester
• CAS NO: 3198-98-9
• Molecular Formula: C13H12N2O4
• Molecular Weight: 260.249
• Mol File: 3198-98-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1H-Pyrazole-3,4-dicarboxylic acid, 1-phenyl-, dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrazole-3,4-dicarboxylic acid, 1-phenyl-, dimethyl ester(3198-98-9)
• EPA Substance Registry System: 1H-Pyrazole-3,4-dicarboxylic acid, 1-phenyl-, dimethyl ester(3198-98-9)

Safety Data

• Hazardous Substances Data: 3198-98-9(Hazardous Substances Data)

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

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

Downstream Products

• 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 
• 892962-79-7 1-(phenyl)-1H-pyrazol-3,4-dicarbohydrazide 

Relevant articles and documents

1,3-dipolar cycloadditions of 3-phenylsydnone with acetylene dicarboxylates in supercritical carbon dioxide

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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

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

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