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Merck
CN

428507

5-(2-Nitrophenyl)furfural

99%

Synonym(s):

5-(2-Nitrophenyl)-2-furancarboxaldehyde

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About This Item

Empirical Formula (Hill Notation):
C11H7NO4
CAS Number:
Molecular Weight:
217.18
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
solid
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Product Name

5-(2-Nitrophenyl)furfural, 99%

InChI

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

SMILES string

[H]C(=O)c1ccc(o1)-c2ccccc2[N+]([O-])=O

InChI key

QBYRUURYXPVDAK-UHFFFAOYSA-N

assay

99%

form

solid

bp

105-107 °C/30 mmHg (lit.)

mp

94-97 °C (lit.)

functional group

aldehyde
nitro

Quality Level

Application

5-(2-Nitrophenyl)furfural (5-(2-nitrophenyl)-2-furfuraldehyde) was used in the synthesis of (5-(2-nitrophenyl)furfuran-2-yl)methanol.
It may be used in the synthesis of 2-{[5-(2-nitrophenyl)furan-2-yl]methyleneamino}benzoic acid (HOBZ) by reacting with 2-aminobenzoic acid.

General description

5-(2-Nitrophenyl)furfural is a furfural derivative.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Ruthenium (II)-Catalyzed Transfer Hydrogenation of Aromatic and Heteroaromatic Aldehydes in Air.
Bhosale SS and Singh KS.
Synthetic Communications, 45(12), 1-10 (2015)
New di-and triorganotin (IV) carboxylates derived from a Schiff base: synthesis, characterization and in vitro antimicrobial activities.
Dias LC, et al.
Applied Organometallic Chemistry, 29(5), 305-313 (2015)

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