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[ CAS No. 25170-73-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 25170-73-4
Chemical Structure| 25170-73-4
Structure of 25170-73-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 25170-73-4 ]

CAS No. :25170-73-4 MDL No. :MFCD19205377
Formula : C6H6F2N2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 144.12 Pubchem ID :-
Synonyms :

Safety of [ 25170-73-4 ]

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Application In Synthesis of [ 25170-73-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 25170-73-4 ]

[ 25170-73-4 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 392-56-3 ]
  • [ 1198-64-7 ]
  • [ 1198-63-6 ]
  • [ 25170-73-4 ]
  • 2,4,5-trifluoro-1,3-phenylenediamine [ No CAS ]
YieldReaction ConditionsOperation in experiment
12 %Chromat. With ammonia In water at 220℃; for 6h; Autoclave;
  • 2
  • [ 1198-63-6 ]
  • [ 25170-73-4 ]
  • 2,4,5-trifluoro-1,3-phenylenediamine [ No CAS ]
YieldReaction ConditionsOperation in experiment
With iron(III) chloride; ammonia; ammonium chloride In water at 200℃; for 6h; Autoclave;
  • 3
  • [ 363-80-4 ]
  • [ 25170-73-4 ]
YieldReaction ConditionsOperation in experiment
72% With ammonia; In 1,4-dioxane; at -33 - 210℃; for 36h;Autoclave; Sealed tube; General procedure: Polyhalogenarene was placed into a steel autoclave equipped with two inlet/outlet valves. The required amount of anhydrous liquid NH3 was added into the autoclave by self-flowing through a measuring funnel with back pressure cooled to -33 C and the autoclave was sealed. The reaction mixture was heated up to the given temperature upon stirring by rotation of the autoclave and kept under these conditions for the necessary time. On completion, the autoclave was cooled, NH3 was slowly vented through an outlet valve, products were extracted with acetone and extract was filtered. Solvent was evaporated to give a crude product, which was then purified. The reactant amounts, reaction conditions, and product yields are listed in Table 1. Methods of isolation of compounds and their characteristics aregiven below.
  • 4
  • [ 17455-13-9 ]
  • [ 25170-73-4 ]
  • C12H24O6*C6H6F2N2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
89% In tert-butyl methyl ether; at 20℃; General procedure: A solutionof 10.6 mmol 18-crown-6 in 10 ml MTBE (for associate -3, in hexane) is added to a solution of 10 mmolpolyhalogenophenylenediamine in 10 ml MTBE (diamine 3 in hexane); the mixture is kept at room temperature and stirredfor ?1-2 h. The fine crystalline precipitate is filtered, washed on a filter with 5 ml MTBE (associate -3 with hexane), anddried in diaphragm pump vacuum (0.5 mm Hg)
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