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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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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