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422916

Sigma-Aldrich

2-Methoxy-4-nitrobenzoic acid

98%

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About This Item

Fórmula lineal:
CH3OC6H3(NO2)CO2H
Número de CAS:
2597-56-0
Peso molecular:
197.14
EC Number:
219-998-6
MDL number:
MFCD00216573
UNSPSC Code:
12352100
PubChem Substance ID:
24866465
NACRES:
NA.22

assay

98%

mp

146-148 °C (lit.)

SMILES string

COc1cc(ccc1C(O)=O)[N+]([O-])=O

InChI

1S/C8H7NO5/c1-14-7-4-5(9(12)13)2-3-6(7)8(10)11/h2-4H,1H3,(H,10,11)

InChI key

KPJXEWJRJKEOCD-UHFFFAOYSA-N

Categorías relacionadas

General description

2-Methoxy-4-nitrobenzoic acid is an alkoxybenzoic acid derivative. It has been reported to be synthesized by reacting 2-hydroxy-4-nitrobenzoic acid with methyl iodide and characterized by 1H and 13C-NMR spectra.

Application

2-Methoxy-4-nitrobenzoic acid may be used as a starting material in the following syntheses:
  • 2-Methoxy-4-nitrobenzamide, a nitroamide derivative.
  • 4-Amino-2-methoxybenzamide, an aminobenzamide derivative.
  • N,2-Dimethoxy-N-methyl-4-nitrobenzamide, a Weinreb amide derivative.
  • 1-(2-Methoxy-4-nitrophenyl)-5-methylhex-2-yn-1-one, a ynone derivative.
  • 2,5-Constrained piperidine derivative, a potential CCR3 (Chemokine (C-C Motif) Receptor 3) antagonist.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Marc J Adler et al.
The Journal of organic chemistry, 76(17), 7040-7047 (2011-07-12)
The design and synthesis of small molecule α-helix mimetics has been a productive field over the past decade. These compounds have performed well in a variety of biological systems as functional disruptors of α-helix-mediated protein-protein interactions. In our studies we
Leyi Gong et al.
Bioorganic & medicinal chemistry letters, 13(20), 3597-3600 (2003-09-25)
As part of our investigation into the development of potent CCR3 antagonists, a series of piperidine analogues was designed and prepared. Exploration of the piperidine core examined both the basicity and the location of a nitrogen, as well as conformational

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