Pyrazole, 99%

Name: Pyrazole, 99% | 288-13-1
Brand: J&K Chemical
SKU: JK258136_250_G
Price: 252.7 USD
Availability: InStock

Cat. No JK258136_250_G

Vendor: J&K Chemical

Product Information

Product Name

Pyrazole, 99%

Brand Name

J&K

Product Number

258136

CAS

288-13-1

Molecular Formula

C3H4N2

Molecular Weight

68.08

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

1,2-Diazole

PubChem CID

1048

IUPAC Name

1H-pyrazole

InChI Key

WTKZEGDFNFYCGP-UHFFFAOYSA-N

SMILES

C1=CNN=C1

Properties

Melting Point

66-70

Boiling Point

186-188

Safety Information

Signal Word

Warning

Hazard Statement

H302

H315

H319

H335

Precautionary Statement

P270

P330

P501

P280

P321

P261

P271

P319

P405

P301+P317

P302+P352

P332+P317

P362+P364

P264+P265

P305+P351+P338

P337+P317

P304+P340

P403+P233

References

Evaluation of innovative promising fungicide from nitropyrazolone class: effects on phytopathogens and non-target organisms

Publication Name: Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]

Publication Date: 2025-09

DOI: 10.1007/s42770-025-01721-x

Synthesis of Fully Substituted 1,2,3-Triazoles via Organocatalytic [3+2] Cycloaddition: Incorporation of Pyrazole and Imidazole Scaffolds as Potent EGFR-Targeted Anticancer Agents

Publication Name: Russian Journal of Bioorganic Chemistry

Publication Date: 2025-07-28

DOI: 10.1134/s1068162024606633

Design, Synthesis, and Molecular Docking of Novel Fluorine-Containing 1,2,3-Triazole-tethered Pyrazole-Chalcone Derivatives as Antimicrobial Agents

Publication Name: Russian Journal of Bioorganic Chemistry

Publication Date: 2025-07-28

DOI: 10.1134/s1068162024606323

Optoelectronic Properties of a Newly Synthesized Electro-Optically Active Heterocyclic Compound Including Pyrazole, Coumarin and Acrylonitrile Groups

Publication Name: Arabian Journal for Science and Engineering

Publication Date: 2025-07-23

DOI: 10.1007/s13369-025-10458-6

Synthesis, spectroscopic characterizations, comparison of experimental, theoretical results, and molecular docking of novel hydrazone Schiff base compound N'-(4-hydroxy-3,5-dimethoxybenzylidene)-1-(2-methoxyphenyl)-5-methyl-1H-pyrazole-4-carbohydrazide

Publication Name: Journal of the Iranian Chemical Society

Publication Date: 2025-07-22

DOI: 10.1007/s13738-025-03251-7

Pyrazole, 99%

Product Information

General Information

Properties

Safety Information

References

Evaluation of innovative promising fungicide from nitropyrazolone class: effects on phytopathogens and non-target organisms

Synthesis of Fully Substituted 1,2,3-Triazoles via Organocatalytic [3+2] Cycloaddition: Incorporation of Pyrazole and Imidazole Scaffolds as Potent EGFR-Targeted Anticancer Agents

Design, Synthesis, and Molecular Docking of Novel Fluorine-Containing 1,2,3-Triazole-tethered Pyrazole-Chalcone Derivatives as Antimicrobial Agents

Optoelectronic Properties of a Newly Synthesized Electro-Optically Active Heterocyclic Compound Including Pyrazole, Coumarin and Acrylonitrile Groups

Synthesis, spectroscopic characterizations, comparison of experimental, theoretical results, and molecular docking of novel hydrazone Schiff base compound N'-(4-hydroxy-3,5-dimethoxybenzylidene)-1-(2-methoxyphenyl)-5-methyl-1H-pyrazole-4-carbohydrazide

Pyrazole, 99%

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Pyrazole, 99%

Product Information

General Information

Properties

Safety Information

References

Evaluation of innovative promising fungicide from nitropyrazolone class: effects on phytopathogens and non-target organisms

Synthesis of Fully Substituted 1,2,3-Triazoles via Organocatalytic [3+2] Cycloaddition: Incorporation of Pyrazole and Imidazole Scaffolds as Potent EGFR-Targeted Anticancer Agents

Design, Synthesis, and Molecular Docking of Novel Fluorine-Containing 1,2,3-Triazole-tethered Pyrazole-Chalcone Derivatives as Antimicrobial Agents

Optoelectronic Properties of a Newly Synthesized Electro-Optically Active Heterocyclic Compound Including Pyrazole, Coumarin and Acrylonitrile Groups

Synthesis, spectroscopic characterizations, comparison of experimental, theoretical results, and molecular docking of novel hydrazone Schiff base compound N'-(4-hydroxy-3,5-dimethoxybenzylidene)-1-(2-methoxyphenyl)-5-methyl-1H-pyrazole-4-carbohydrazide

Pyrazole, 99%

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