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2-Fluorobenzohydrazide

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2-Fluorobenzohydrazide Basic information

Product Name:
2-Fluorobenzohydrazide
Synonyms:
  • 2-Fluorobenzhydrazide,99%
  • 2-Fluorobenzhydrazide 98%
  • 2-Fluorobenzhydrazide98%
  • o-Fluorobenzohydrazide
  • 2 flurobenzhydrazide
  • 2-Fluorobenzoic hydrazide,2 Flurobenzhydrazide
  • 2-Fluorobenzoylhydrazine 2-Fluorobenzoic Hydrazide
  • 2-FLUOROBENZOIC HYDRAZIDE
CAS:
446-24-2
MF:
C7H7FN2O
MW:
154.14
Product Categories:
  • Aromatic Hydrazides, Hydrazines, Hydrazones and Oximes
  • Miscellaneous
  • Fluorine Compounds
  • Fluorine series
Mol File:
446-24-2.mol
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2-Fluorobenzohydrazide Chemical Properties

Melting point:
70-74 °C (lit.)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
soluble in Methanol
form 
Powder or Crystalline Powder
color 
White to pale brown
CAS DataBase Reference
446-24-2(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 
2928009090

MSDS

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2-Fluorobenzohydrazide Usage And Synthesis

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 26, p. 257, 1989 DOI: 10.1002/jhet.5570260147

Synthesis

443-26-5

446-24-2

GENERAL METHODS: 2-Fluorophenylidene hydrazine was synthesized routinely by one-pot method (30-58% yield). Ethyl o-fluorobenzoate (10 mmol) was dissolved in ethanol (20 mL). 3N sulfuric acid (2 mL) was added to the solution, followed by refluxing the reaction mixture for 6 hours. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was neutralized with solid NaHCO3 and excess NaHCO3 was removed by filtration.To the neutralized reaction mixture, hydrazine monohydrate (1.5 mL, 3 mmol) was added and refluxing was continued for 3-6 h to ensure complete reaction. The ethanol and unreacted hydrazine monohydrate were concentrated to 1/3 of the original volume by distillation.The reaction mixture was cooled to room temperature, the resulting solid was filtered and recrystallized from methanol to give crystals of the target product, 2-fluorophenylidenehydrazine (see Supporting Information for specific data).

References

[1] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 17, p. 6014 - 6024
[2] Journal of the American Chemical Society, 1950, vol. 72, p. 1806
[3] Journal of Agricultural and Food Chemistry, 2003, vol. 51, # 1, p. 152 - 155
[4] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 8, p. 2278 - 2282
[5] Journal of Medicinal Chemistry, 2010, vol. 53, # 20, p. 7392 - 7404

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