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428507

Sigma-Aldrich

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
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

solid

bp

105-107 °C/30 mmHg (lit.)

mp

94-97 °C (lit.)

SMILES string

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

InChI

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

InChI key

QBYRUURYXPVDAK-UHFFFAOYSA-N

General description

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

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.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

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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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)
Ruthenium (II)-Catalyzed Transfer Hydrogenation of Aromatic and Heteroaromatic Aldehydes in Air.
Bhosale SS and Singh KS.
Synthetic Communications, 45(12), 1-10 (2015)

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