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[ CAS No. 65535-53-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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Chemical Structure| 65535-53-7
Chemical Structure| 65535-53-7
Structure of 65535-53-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 65535-53-7 ]

CAS No. :65535-53-7 MDL No. :MFCD04039913
Formula : C9H8FNO Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 165.16 Pubchem ID :-
Synonyms :

Safety of [ 65535-53-7 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P284-P301+P310+P330-P302+P352+P332+P313+P362+P364-P304+P340+P311-P305+P351+P338+P337+P313 UN#:2206
Hazard Statements:H301+H331-H315-H319-H334-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 65535-53-7 ]

* 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 [ 65535-53-7 ]

[ 65535-53-7 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 288401-44-5 ]
  • [ 65535-53-7 ]
  • 2,4-dichloro-2-(isoxazol-5-yl)phenyl 4-fluorophenethylcarbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
71% With triethylamine In toluene Heating;
  • 2
  • [ 1996-41-4 ]
  • [ 65535-53-7 ]
  • 4-chloro-2-fluorophenyl 4-fluorophenethylcarbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
77% With triethylamine In toluene Heating;
  • 3
  • [ 65535-53-7 ]
  • [ 86176-56-9 ]
  • 4-chloro-2-(isoxazol-5-yl)phenyl 4-fluorophenethylcarbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
78% With triethylamine In toluene Heating;
  • 4
  • [ 452-70-0 ]
  • [ 65535-53-7 ]
  • 4-fluoro-3-methylphenyl 4-fluorophenethylcarbamate [ No CAS ]
  • 5
  • [ 89-68-9 ]
  • [ 65535-53-7 ]
  • 4-chloro-2-isopropyl-5-methylphenyl 4-fluorophenethylcarbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
75% With triethylamine In toluene Heating;
  • 6
  • [ 1563-38-8 ]
  • [ 65535-53-7 ]
  • 2,2-dimethyl-2,3-dihydrobenzofuran-7-yl 4-fluorophenethylcarbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
69% With triethylamine In toluene Heating;
  • 7
  • [ 94-71-3 ]
  • [ 65535-53-7 ]
  • 2-ethoxyphenyl 4-fluorophenethylcarbamate [ No CAS ]
  • 8
  • [ 65535-53-7 ]
  • [ 93246-53-8 ]
  • 1-[3-fluoro-4-(morpholin-4-yl)phenyl]-3-[2-(4-fluorophenyl)ethyl]urea [ No CAS ]
YieldReaction ConditionsOperation in experiment
22% In tetrahydrofuran; at 40 - 45℃; for 24h; A THF solution (20 ml) of 1- (2-isocyanatoethyl) -4-fluorobenzene (1.51 mmol) and 3-fluoro-4-morpholinoaniline (1.51 mmol)Stir at 40-45 C for 24 hours. The next day, the completion of the reaction was confirmed by TLC. The solvent was distilled off and ammonium chloride (100 ml), water (50 ml) and ethyl acetate (100 ml) were added to the remaining residue. The organic layer was treated with brine and dried over sodium sulfate. The solvent was distilled off and the resulting concentrate was adsorbed onto silica gel using methylene chloride. The mixture was purified by column chromatography using ethyl acetate in hexane to give the title compound.
22% In tetrahydrofuran; at 40 - 45℃; for 24h; A THF solution (20 ml) of 1- (2-isocyanatoethyl) -4-fluorobenzene (1.51 mmol) and 3-fluoro-4-morpholinoaniline (20 ml) 40-45 C. The next day completion of the reaction was confirmed by TLC. The solvent was distilled off and ammonium chloride (100 ml), water (50 ml) and ethyl acetate (100 ml) were added to the remaining residue. Brine organic layer Lt; / RTI & gt; and dried over sodium sulfate. The solvent was distilled off and the resulting concentrate was adsorbed onto silica gel using methylene chloride. The mixture was purified by column chromatography using ethyl acetate in hexane to give the title compound.
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