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Sigma-Aldrich

4-Hydroxy-3-nitrobenzaldehyde

97%

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About This Item

Linear Formula:
HOC6H3(NO2)CHO
CAS Number:
3011-34-5
Molecular Weight:
167.12
Beilstein:
2047884
EC Number:
221-141-6
MDL number:
MFCD00007117
UNSPSC Code:
12352100
PubChem Substance ID:
24848648
NACRES:
NA.22

Quality Level

100

Assay

97%

mp

140-142 °C (lit.)

SMILES string

[H]C(=O)c1ccc(O)c(c1)[N+]([O-])=O

InChI

1S/C7H5NO4/c9-4-5-1-2-7(10)6(3-5)8(11)12/h1-4,10H

InChI key

YTHJCZRFJGXPTL-UHFFFAOYSA-N

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General description

4-Hydroxy-3-nitrobenzaldehyde reacts with 3-bromo­benzohydrazide in methanol to yield (E)-3-bromo-N′-(4-hydroxy-3-nitrobenzylidene)benzohydrazide.

Application

4-Hydroxy-3-nitrobenzaldehyde was used in the synthesis of:
  • 4-hydroxy-3-nitrocinnamic acid
  • solvated benzohydrazone derivatives: N′-(4-hydroxy-3-nitrobenzylidene)-3-methylbenzohydrazide-methanol-water

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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Characterization and crystal structures of solvated N'-(4-hydroxy-3-nitrobenzylidene)-3-methylbenzohydrazide and N'-(4-dimethyl-aminobenzylidene)-3-methylbenzohydrazide.
Ma, J-J.
Journal of Structural Chemistry, 54(6), 1145-1150 (2013)
Yasuko Sakihama et al.
FEBS letters, 553(3), 377-380 (2003-10-24)
Peroxynitrite (ONOO(-)), a reactive nitrogen species, is capable of nitrating tyrosine residue of proteins. Here we show in vitro evidence that plant phenolic compounds can also be nitrated by an ONOO(-)-independent mechanism. In the presence of NaNO(2), H(2)O(2), and horseradish
Guo-Biao Cao et al.
Acta crystallographica. Section E, Structure reports online, 65(Pt 8), o1725-o1725 (2009-01-01)
The title compound, C(14)H(10)BrN(3)O(4), was synthesized by the reaction of 4-hydr-oxy-3-nitro-benzaldehyde with an equimolar quantity of 3-bromo-benzohydrazide in methanol. The mol-ecule displays an E configuration about the C=N bond. The dihedral angle between the two benzene rings is 4.6 (2)°. The

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