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Chemical Structure| 1377582-58-5 Chemical Structure| 1377582-58-5

Structure of 1377582-58-5

Chemical Structure| 1377582-58-5

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Product Details of [ 1377582-58-5 ]

CAS No. :1377582-58-5
Formula : C7H5F3N2O5S
M.W : 286.19
SMILES Code : O=S(C1=CC=C(OC(F)(F)F)C([N+]([O-])=O)=C1)(N)=O
MDL No. :MFCD28801852

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Application In Synthesis of [ 1377582-58-5 ]

* 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 [ 1377582-58-5 ]

[ 1377582-58-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1644-88-8 ]
  • [ 1377582-58-5 ]
YieldReaction ConditionsOperation in experiment
Intermediate 22: Step a3-Nitro-4-trifluoromethoxy-benzenesulfonamide To chlorosulfonic acid (11.3 mL, 170 mmol) was slowly added commercially available <strong>[1644-88-8]2-trifluoromethoxy-nitrobenzene</strong> (8 g, 38.6 mmol). The reaction mixture was heated at 120 C. for 4 h and then cooled down. The above crude mixture was added to a stirred solution of conc. aq. NH4OH (34.7 mL, 514 mmol, 14.8 M) in iPrOH (100 mL) at -45 C. dropwise over 30 min. The reaction mixture was stirred at -45 C. for 1 h, and 2 N HCl was added to acidify the mixture. Concentration to remove iPrOH was followed by suspension in water, and filtration of the solid. The solid was washed successively with 1 N HCl and water, then air dried to yield the title compound as a white solid.
Intermediate 30: Step a 3-Nitro-4-trifluoromethoxy-benzenesulfonamide To chlorosulfonic acid (11.3 mL, 170 mmol) was slowly added commercially available <strong>[1644-88-8]2-trifluoromethoxy-nitrobenzene</strong> (8 g, 38.6 mmol). The reaction mixture was heated at 120 C. for 4 h and then cooled down. The above crude mixture was added to a stirred solution of conc. aq. NH4OH (34.7 mL, 514 mmol, 14.8 M) in iPrOH (100 mL) at -45 C. dropwise over 30 min. The reaction mixture was stirred at -45 C. for 1 h, and 2 N HCl was added to acidify the mixture. Concentration to remove iPrOH was followed by suspension in water, and filtration of the solid. The solid was washed successively with 1 N HCl and water, then air dried to yield the title compound as a white solid.
Intermediate 62: Step a 3-Nitro-4-trifluoromethoxy-benzenesulfonamide To chlorosulfonic acid (11.3 mL, 170 mmol) was slowly added commercially available <strong>[1644-88-8]2-trifluoromethoxy-nitrobenzene</strong> (8 g, 38.6 mmol). The reaction mixture was heated at 120 C. for 4 h and then cooled down. The above crude mixture was added to a stirred solution of conc. aq. NH4OH (34.7 mL, 514 mmol, 14.8 M) in iPrOH (100 mL) at -45 C. dropwise over 30 min. The reaction mixture was stirred at -45 C. for 1 h, and 2 N HCl was added to acidify the mixture. Concentration to remove iPrOH was followed by suspension in water, and filtration of the solid. The solid was washed successively with 1 N HCl and water, then air dried to yield the title compound as a white solid.
To chlorosulfonic acid (11.3 mL, 170 mmol) was slowly added commercially available <strong>[1644-88-8]2-trifluoromethoxy-nitrobenzene</strong> (8 g, 38.6 mmol). The reaction mixture was heated at 120 C. for 4 h and then cooled down. The above crude mixture was added to a stirred solution of conc. aq. NH4OH (34.7 mL, 514 mmol, 14.8 M) in iPrOH (100 mL) at -45 C. dropwise over 30 min. The reaction mixture was stirred at -45 C. for 1 h, and 2 N HCl was added to acidify the mixture. Concentration to remove iPrOH was followed by suspension in water, and filtration of the solid. The solid was washed successively with 1 N HCl and water, then air dried to yield the title compound as a white solid.
To chlorosulfonic acid (11.3 mL, 170 mmol) was slowly added commercially available <strong>[1644-88-8]2-trifluoromethoxy-nitrobenzene</strong> (8 g, 38.6 mmol). The reaction mixture was heated at 120 C. for 4 h and then cooled down. The above crude mixture was added to a stirred solution of conc. aq. NH4OH (34.7 mL, 514 mmol, 14.8 M) in iPrOH (100 mL) at -45 C. dropwise over 30 min. The reaction mixture was stirred at -45 C. for 1 h, and 2 N HCl was added to acidify the mixture. Concentration to remove iPrOH was followed by suspension in water, and filtration of the solid. The solid was washed successively with 1 N HCl and water, then air dried to yield the title compound as a white solid.

 

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