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3-(4-Fluorophenyl)-1H-pyrazole-4-carbaldehyde, 97%|250171|306936-57-2

3-(4-Fluorophenyl)-1H-pyrazole-4-carbaldehyde, 97%

Cat. No JK250171_5_G
J&K Chemical

Product Information

Product Name
3-(4-Fluorophenyl)-1H-pyrazole-4-carbaldehyde, 97%
Brand Name
J&K
Product Number
250171
CAS
306936-57-2
Molecular Formula
C10H7FN2O
Molecular Weight
190.17
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
605439
IUPAC Name
5-(4-fluorophenyl)-1H-pyrazole-4-carbaldehyde
InChI Key
CMXTUUXWJBLVEH-UHFFFAOYSA-N
SMILES
C1=CC(=CC=C1C2=C(C=NN2)C=O)F

Properties

Melting Point
154-155

Safety Information

Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Application of the concept of oxime library screening by mass spectrometry (MS) binding assays to pyrrolidine-3-carboxylic acid derivatives as potential inhibitors of γ-aminobutyric acid transporter 1 (GAT1)
Publication Name: Bioorganic & Medicinal Chemistry
Publication Date: 2019-07-01
DOI: 10.1016/j.bmc.2019.05.001

Screening oxime libraries by means of mass spectrometry (MS) binding assays: Identification of new highly potent inhibitors to optimized inhibitors γ-aminobutyric acid transporter 1
Publication Name: Bioorganic & Medicinal Chemistry
Publication Date: 2019-04-01
DOI: 10.1016/j.bmc.2019.02.015

Synthesis of new methyl derivatives of aza-and diazaphenanthrene
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2008-07
DOI: 10.1134/s1070428008070178

3-(4-fluorophenyl)-1H-pyrazole-4-carbaldehyde in the synthesis of aza-and diazaphenanthrene derivatives
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2007-02
DOI: 10.1134/s1070428007020157

Cascade heterocyclization of 2-naphthylamine with substituted benzaldehydes and acetophenones
Publication Name: Russian Journal of General Chemistry
Publication Date: 2006-11
DOI: 10.1134/s1070363206110259

3-(4-Fluorophenyl)-1H-pyrazole-4-carbaldehyde, 97%

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