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2,4-DIAMINOFLUOROBENZENE

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2,4-DIAMINOFLUOROBENZENE Basic information

Product Name:
2,4-DIAMINOFLUOROBENZENE
Synonyms:
  • 5-AMINO-2-FLUOROANILINE
  • 4-FLUORO-BENZENE-1,3-DIAMINE
  • 4-FLUORO-1,3-PHENYLENEDIAMINE
  • 4-Fluoro-1,3-benzenediamine
  • 2,4-DIAMINOFLUOROBENZENE
  • 4-Fluoro-1,3-diaminobenzene, 95%
  • 1,3-DIAMINO-4-FLUOROBENZENE
  • 1,2-DiaMino-4-difluorobenzene
CAS:
6264-67-1
MF:
C6H7FN2
MW:
126.13
EINECS:
228-426-4
Product Categories:
  • Anilines, Aromatic Amines and Nitro Compounds
Mol File:
6264-67-1.mol
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2,4-DIAMINOFLUOROBENZENE Chemical Properties

Melting point:
34-37 °C(lit.)
Boiling point:
152-153 °C(lit.)
Density 
1.284±0.06 g/cm3(Predicted)
Flash point:
221 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
4.65±0.10(Predicted)
form 
Powder
color 
Black
CAS DataBase Reference
6264-67-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
2921599090

MSDS

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2,4-DIAMINOFLUOROBENZENE Usage And Synthesis

Synthesis

364-76-1

6264-67-1

In Example 1, equimolar 4-fluoro-3-nitroaniline was substituted for m-nitroacetophenone as a raw material, and the reaction conditions were set at 80°C and 4.0 MPa for 48 hours. The rest of the operation steps were kept consistent with Example 1, and 4-fluoro-1,3-diaminobenzene was finally obtained in 94% yield. The specific operation was as follows: 16.44 mg (0.04 mmol) of silver 4,4'-dimethoxy-2,2'-bipyridine, 11.22 mg (0.1 mmol) of potassium tert-butoxide and 1 mL of 1,4-dioxane were added to an autoclave. After thorough stirring, 165.15 mg (1 mmol) of m-nitroacetophenone was added and the mixture was stirred continuously at 80 °C for 8 hours. Upon completion of the reaction, the organic phase was separated by extraction of the reaction solution using water and dichloromethane. The organic phase was subsequently dried with anhydrous Na2SO4 and purified by filtration, rotary evaporation and chromatographic separation to afford 3-acetanilide as a yellow solid in 96% yield.

References

[1] Patent: CN106748834, 2017, A. Location in patent: Paragraph 0016; 0069; 0072
[2] Patent: US4552882, 1985, A

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