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5-Phenyl-1H-pyrazole-3-carboxylic acid, 97%|264726|1134-49-2

5-Phenyl-1H-pyrazole-3-carboxylic acid, 97%

Cat. No JK264726_1_G
J&K Chemical

Product Information

Product Name
5-Phenyl-1H-pyrazole-3-carboxylic acid, 97%
Brand Name
J&K
Product Number
264726
CAS
1134-49-2
Molecular Formula
C10H8N2O2
Molecular Weight
188.19
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
121025
IUPAC Name
3-phenyl-1H-pyrazole-5-carboxylic acid
InChI Key
QBPUOAJBMXXBNU-UHFFFAOYSA-N
SMILES
C1=CC=C(C=C1)C2=NNC(=C2)C(=O)O

Properties

Melting Point
238-242

Safety Information

Signal Word
Warning
Hazard Statement
H316
H320
H335
Precautionary Statement
P261
P271
P319
P405
P501
P332+P317
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

A quantitative high-throughput screen identifies compounds that lower expression of the SCA2-and ALS-associated gene ATXN2
Publication Name: The Journal of biological chemistry
Publication Date: 2022-08
DOI: 10.1016/j.jbc.2022.102228

Discovery of small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase
Publication Name: Journal of Enzyme Inhibition and Medicinal Chemistry
Publication Date: 2022-05-05
DOI: 10.1080/14756366.2022.2070909

Pyrrolyl Pyrazoles as Non-Diketo Acid Inhibitors of the HIV-1 Ribonuclease H Function of Reverse Transcriptase
Publication Name: ACS Medicinal Chemistry Letters
Publication Date: 2020-03-05
DOI: 10.1021/acsmedchemlett.9b00617

Discovery of Membrane-Bound Pyrophosphatase Inhibitors Derived from an Isoxazole Fragment
Publication Name: ACS Medicinal Chemistry Letters
Publication Date: 2020-02-17
DOI: 10.1021/acsmedchemlett.9b00537

Synthesis of 4-aryl(hetaryl)pyrazolo[1,5-a]pyrazines by palladium-catalyzed Suzuki–Miyaura cross coupling
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2019-11-25
DOI: 10.1007/s10593-019-02579-2

5-Phenyl-1H-pyrazole-3-carboxylic acid, 97%

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