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527424

Sigma-Aldrich

2-Hydroxy-3-nitrobenzaldehyde

98%

Synonym(s):

3-Nitrosalicylaldehyde

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About This Item

Linear Formula:
HOC6H3(NO2)CHO
CAS Number:
Molecular Weight:
167.12
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

mp

105-109 °C (lit.)

SMILES string

Oc1c(C=O)cccc1[N+]([O-])=O

InChI

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

InChI key

NUGOTBXFVWXVTE-UHFFFAOYSA-N

General description

2-Hydroxy-3-nitrobenzaldehyde can be extracted from the leaves of Actephila merrilliana. Its molecule is planar. On reaction with dapsone, it affords a colorless solution.

Application

2-Hydroxy-3-nitrobenzaldehyde may be used in the synthesis of 5-acetyl-4-aryl-6-methyl-1,2,3,4-tetrahydro pyrimidine.

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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Dapsone assay based on Schiff base formation.
Levy L and Higgins LJ.
Blood, 4(2) (1966)
2-Hydroxy-3-nitrobenzaldehyde.
Tang B, et al.
Acta Crystallographica Section E, Structure Reports Online, 66(8), o1912-o1912 (2010)
Synthesis of new 4-aryl-isoxazolo [5, 4-d] pyrimidin-6-one (thione) and 4-aryl-pyrazolo [3, 4-d]-pyrimidin-6-one derivatives of potential antihypertensive activity.
El-Hamouly WS, et al.
Indian J. Chem. B, 45(9), 2091-2091 (2006)

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