Basic information Safety Supplier Related

4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98

Basic information Safety Supplier Related

4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98 Basic information

Product Name:
4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98
Synonyms:
  • 4-Bromo-5-fluoro-o-phenylenediamine
  • 4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98
  • 4-Bromo-5-fluoro-1,2-phenylenediamine 98%
  • 4-Bromo-5-fluorobenzene-1,2-diamine 97%
  • 4-Bromo-5-fluorophenylene-1,2-diamine, 4-Bromo-1,2-diamino-5-fluorobenzene
  • 1,2-BenzenediaMine, 4-broMo-5-fluoro-
  • 4-Bromo-5-fluorophenylene-1,2-diamine, 1-Bromo-4,5-diamino-2-fluorobenzene
  • 4-Bromo-5-fluorobenzene-1,2-diamine97%
CAS:
153505-37-4
MF:
C6H6BrFN2
MW:
205.03
Mol File:
153505-37-4.mol
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4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98 Chemical Properties

Boiling point:
297.0±35.0 °C(Predicted)
Density 
1.792±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
3.15±0.10(Predicted)
form 
powder
color 
Brown
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2921511990
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4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98 Usage And Synthesis

Synthesis

153505-36-3

153505-37-4

General procedure for the synthesis of 4-bromo-5-fluoro-2-nitroaniline from 4-bromo-5-fluoro-2-nitroaniline: to a solution of 4-bromo-5-fluoro-2-nitroaniline (1.0 g, 4.3 mmol) in THF (9.0 mL) was added EtOH (9.0 mL) and H2O (3 mL), followed by the addition of iron powder (1.2 g, 21.3 mmol) and ammonium chloride (0.34 g, 6.4 mmol). The reaction mixture was heated to reflux at 95 °C for 4 hours. After completion of the reaction, the mixture was cooled to room temperature, diluted with EtOH and filtered through a diatomaceous earth pad until the filtrate was colorless. The filtrate was concentrated under reduced pressure, the residue was dissolved in EtOAc, washed sequentially with H2O and brine, the organic phase was dried with anhydrous Na2SO4, filtered and concentrated. Hexane was added to the concentrate and the precipitated solid was collected by filtration to afford the title compound 4-bromo-5-fluorobenzene-1,2-diamine (710 mg, 3.5 mmol, 81% yield).

References

[1] Patent: EP2566477, 2015, B1. Location in patent: Paragraph 0172; 0173
[2] Patent: WO2012/83170, 2012, A1. Location in patent: Page/Page column 155
[3] Patent: WO2013/26914, 2013, A1. Location in patent: Page/Page column 134
[4] Patent: US2007/259936, 2007, A1. Location in patent: Page/Page column 175
[5] Patent: US2010/222345, 2010, A1. Location in patent: Page/Page column 69

4-BROMO-5-FLUORO-1,2-PHENYLENEDIAMINE 98Supplier

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