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Sigma-Aldrich

5-(4-Nitrophenyl)furfural

98%

Synonym(s):

5-(4-Nitrophenyl)-2-furancarboxaldehyde

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About This Item

Empirical Formula (Hill Notation):
C11H7NO4
CAS Number:
Molecular Weight:
217.18
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

assay

98%

form

solid

mp

204-206 °C (lit.)

SMILES string

[H]C(=O)c1ccc(o1)-c2ccc(cc2)[N+]([O-])=O

InChI

1S/C11H7NO4/c13-7-10-5-6-11(16-10)8-1-3-9(4-2-8)12(14)15/h1-7H

InChI key

RTSOJVJDKNKNFU-UHFFFAOYSA-N

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General description

5-(4-Nitrophenyl)furfural is a furfural nitrophenyl derivative.

Application

5-(4-Nitrophenyl)furfural was used in the synthesis of (E)-methyl 3-(5-(4-nitrophenyl)furan-2-yl)acrylate.
It may be used in the synthesis of 2-[5(6)-{N-isopropylamidino}-2-benzimidazoyl]-5-(4-nitrophenyl)furan and 2-[(3-methylquinoxalin-2-yl)oxy]-N′-(1E)-[5-(4-nitrophenyl)-2-furfuryl]methyleneacetohydrazide, a quinoxaline-incorporated Schiff base.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


Certificates of Analysis (COA)

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M Daniel Givens et al.
Antimicrobial agents and chemotherapy, 47(7), 2223-2230 (2003-06-25)
Bovine viral diarrhea virus (BVDV) is an economically significant pathogen of cattle and a problematic contaminant in the laboratory. BVDV is often used as an in vitro model for hepatitis C virus during drug discovery efforts. Aromatic dicationic molecules have
Microwave-Assisted Synthesis of Some Quinoxaline-Incorporated Schiff Bases and Their Biological Evaluation.
Achutha L, et al.
Journal of Chemistry, 2013 (2012)
Jesus Vazquez et al.
Journal of medicinal chemistry, 50(9), 2137-2143 (2007-03-31)
We report on the design, synthesis, and evaluation of a series of furanyl-salicyl-nitroxide derivatives as effective chemical probes for second-site screening against phosphotyrosine phosphatases (PTPs) using NMR-based techniques. The compounds have been tested against a panel of PTPs to assess

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