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2-Fluorophenylhydrazine

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Company Name: Henan Fengda Chemical Co., Ltd
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Products Intro: Product Name:2-Fluorophenylhydrazine
CAS:2368-80-1
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CAS:2368-80-1
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CAS: 2368-80-1
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Products Intro: Product Name:(2-Fluorophenyl)hydrazine
CAS:2368-80-1
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Products Intro: Product Name:2-fluorophenylhydrazine
CAS:2368-80-1
Purity:0.99 Package:1kg

2-Fluorophenylhydrazine manufacturers

  • 2-Fluorophenylhydrazine
  • 2-Fluorophenylhydrazine pictures
  • $100.00 / 1KG
  • 2025-09-25
  • CAS:2368-80-1
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: g-kg-tons, free sample is available
2-Fluorophenylhydrazine Basic information
Product Name:2-Fluorophenylhydrazine
Synonyms:2-FLUOROPHENYLHYDRAZINE;1-(2-fluorophenyl)hydrazine;2-Fluoropherylhydrazine;ASINEX-REAG BAS 05500094;o-Fluorophenylhydrazine;2-Fluorophenylhrazine;1-fluoro-1-phenylhydrazine;Hydrazine, (2-fluorophenyl)-
CAS:2368-80-1
MF:C6H7FN2
MW:126.13
EINECS:220-886-4
Product Categories:Aromatic Hydrazides, Hydrazines, Hydrazones and Oximes;Fluorobenzene;Phenylhydrazine
Mol File:2368-80-1.mol
2-Fluorophenylhydrazine Structure
2-Fluorophenylhydrazine Chemical Properties
Melting point 47°C
Boiling point 76-79°C/3mm
density 1.257±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
pka4.73±0.10(Predicted)
form solid
color White to tan
CAS DataBase Reference2368-80-1(CAS DataBase Reference)
EPA Substance Registry SystemHydrazine, (2-fluorophenyl)- (2368-80-1)
Safety Information
Hazard Codes Xi
TSCA TSCA listed
HS Code 2928009090
MSDS Information
2-Fluorophenylhydrazine Usage And Synthesis
Synthesis
2-Fluoroaniline

348-54-9

2-Fluorophenylhydrazine

2368-80-1

General procedure for the synthesis of 2-fluorophenylhydrazine from o-fluoroaniline: 500 g of o-fluoroaniline and 1500 mL of 37% concentrated hydrochloric acid were added to a 10 L three-necked flask and cooled to 2 °C using an ice-salt bath. 857 g of 35% aqueous sodium nitrite solution was added slowly and dropwise under stirring, and the reaction temperature was controlled to be maintained at 0 to 5 °C for 1.5 hours. Subsequently, 730 mL of 37% concentrated hydrochloric acid, 730 mL of water, and 480 g of zinc powder were added to the reaction solution, and the reaction temperature was maintained at 18 °C until the reaction was complete and the reaction solution turned off-white. Then, 30% sodium hydroxide solution was slowly added to adjust the pH of the reaction solution to 10.5, and this process took about 2 hours, and then crystals were precipitated, and 295 g of 2-fluorophenylhydrazine crude product was obtained by filtration. Purification step: 295 g of 2-fluorophenylhydrazine crude was dissolved in 5900 mL of water, heated to 60 ℃ to make it completely dissolved, and added appropriate amount of activated carbon to decolorize for 20 minutes, and then thermo-filtered to obtain a colorless filtrate. The filtrate was allowed to stand for 5 hours and then continued to stand for 2 hours, and the precipitated crystal precipitate was collected by filtration to finally obtain 238g of purified 2-fluorophenylhydrazine.

References[1] Journal of Medicinal Chemistry, 1991, vol. 34, # 9, p. 2892 - 2898
[2] Chemistry - An Asian Journal, 2015, vol. 10, # 8, p. 1618 - 1621
[3] Molecules, 2016, vol. 21, # 11,
[4] Patent: CN106518723, 2017, A. Location in patent: Paragraph 0037-0046
[5] Patent: CN106518714, 2017, A. Location in patent: Paragraph 0017 - 0023
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