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2-Fluoro-5-nitrobenzoic acid

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2-Fluoro-5-nitrobenzoic acid Basic information

Product Name:
2-Fluoro-5-nitrobenzoic acid
Synonyms:
  • 2-FLUORO-5-NITROBENZOIC ACID
  • RARECHEM AL BO 0445
  • BUTTPARK 32\01-76
  • 2-Fluoro-5-nitrobenzoic acid 98%
  • 2-Fluoro-5-nitrobenzoicacid98%
  • 2-FLUORO-5-NITRROBENZOIC ACID
  • 2-Fluoro-5-nitrobenzotc acid
  • NSC 133450
CAS:
7304-32-7
MF:
C7H4FNO4
MW:
185.11
EINECS:
627-772-7
Product Categories:
  • Aromatics
  • Miscellaneous Reagents
  • C7
  • Carbonyl Compounds
  • Carboxylic Acids
  • Benzoic acid series
  • Fluorobenzene
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • Benzoic acid
  • Fluorobenzoic acids
Mol File:
7304-32-7.mol
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2-Fluoro-5-nitrobenzoic acid Chemical Properties

Melting point:
142-144 °C (lit.)
Boiling point:
337.7±27.0 °C(Predicted)
Density 
1.568±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Soluble in chloroform, ethanol.
pka
2.54±0.10(Predicted)
form 
Crystalline Powder
color 
White to pale yellow
BRN 
1912835
CAS DataBase Reference
7304-32-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29163990

MSDS

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2-Fluoro-5-nitrobenzoic acid Usage And Synthesis

Chemical Properties

white to light yellow crystal powder

Uses

2-Fluoro-5-nitrobenzoic acid may be used in the synthesis of dibenz[b,f]oxazepin-11(10H)-ones, via the nucleophilic aromatic substitution (SNAr) of fluorine in 2-fluoro-5-nitrobenzoic acid with the OH of various 2-aminophenols on solid support, synthesis of substituted dibenzazocines on solid support, via SNAr of fluorine in 2-fluoro-5-nitrobenzoic acid with the OH function of the immobilized polysubstituted phenols, in the synthesis of oxazepines.

Uses

2-Fluoro-5-nitrobenzoic acid may be used in the synthesis of:

  • dibenz[b,f]oxazepin-11(10H)-ones, via the nucleophilic aromatic substitution (SNAr) of fluorine in 2-fluoro-5-nitrobenzoic acid with the OH of various 2-aminophenols on solid support
  • synthesis of substituted dibenzazocines on solid support, via SNAr of fluorine in 2-fluoro-5-nitrobenzoic acid with the OH function of the immobilized polysubstituted phenols
  • in the synthesis of oxazepines

General Description

2-Fluoro-5-nitrobenzoic acid is reported to react with an aldehyde, isonitrile and a primary amine tethered to a Boc-protected internal amino or hydroxyl nucleophile, to afford the Ugi product.

2-Fluoro-5-nitrobenzoic acid Supplier

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