Basic information Safety Supplier Related

2-Methoxy-4-nitrobenzoic acid

Basic information Safety Supplier Related

2-Methoxy-4-nitrobenzoic acid Basic information

Product Name:
2-Methoxy-4-nitrobenzoic acid
Synonyms:
  • 4-NITRO-2-METHOXYBENZOIC ACID
  • 4-Nitro-o-anisic acid
  • RARECHEM AL BO 1464
  • 2-METHOXY-4-NITROBENZOIC ACID
  • 2-Methoxy-4-nitrobenzoid acid
  • 2-Carboxy-5-nitroanisole
  • NSC 229300
  • 2-Methoxy-4-nitrobenzoic acid 98%
CAS:
2597-56-0
MF:
C8H7NO5
MW:
197.14
EINECS:
219-998-6
Product Categories:
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • Benzoic acid
  • Aromatics Compounds
  • Aromatics
  • C8
  • Carbonyl Compounds
  • Carboxylic Acids
Mol File:
2597-56-0.mol
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2-Methoxy-4-nitrobenzoic acid Chemical Properties

Melting point:
146-148 °C (lit.)
Boiling point:
390.9±27.0 °C(Predicted)
Density 
1.430±0.06 g/cm3(Predicted)
solubility 
Acetic Acid, Methanol
form 
Solid
pka
3.13±0.13(Predicted)
color 
White to Off-White
CAS DataBase Reference
2597-56-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29189900

MSDS

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2-Methoxy-4-nitrobenzoic acid Usage And Synthesis

Chemical Properties

White to Off-White Crystalline Solid

Uses

2-Methoxy-4-nitrobenzoic Acid (cas# 2597-56-0) is a compound useful in organic synthesis.

Uses

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.

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.

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