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C45H42F5N5O18S2

Base Information
  • Chemical Name:C45H42F5N5O18S2
  • CAS No.:178447-05-7
  • Molecular Formula:C45H42F5N5O18S2
  • Molecular Weight:1099.98
  • Hs Code.:
C<sub>45</sub>H<sub>42</sub>F<sub>5</sub>N<sub>5</sub>O<sub>18</sub>S<sub>2</sub>

Synonyms:C45H42F5N5O18S2

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Chemical Property of C45H42F5N5O18S2
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Technology Process of C45H42F5N5O18S2

There total 7 articles about C45H42F5N5O18S2 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With acetic acid; at 70 ℃; for 7h;
DOI:10.1039/p19960000985
Guidance literature:
Multi-step reaction with 3 steps
1: 75 percent / DCC / ethyl acetate / Ambient temperature
2: 98 percent / molecular sieves 4 Angstroem, TMSOTf / CH2Cl2 / 1.) 0 deg C, 10 min, 2.) 0 deg C, 30 min
3: 98 percent / 80percent aq. AcOH / 7 h / 70 °C
With trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; acetic acid; dicyclohexyl-carbodiimide; In dichloromethane; ethyl acetate;
DOI:10.1039/p19960000985
Guidance literature:
Multi-step reaction with 6 steps
1: 94 percent / HCO2H / 12 h / Ambient temperature
2: 65 percent / N2H4*H2O / methanol / 7.5 h / Ambient temperature
3: 73 percent / p-TsOH / nitromethane / 3 h / Ambient temperature
4: 75 percent / DCC / ethyl acetate / Ambient temperature
5: 98 percent / molecular sieves 4 Angstroem, TMSOTf / CH2Cl2 / 1.) 0 deg C, 10 min, 2.) 0 deg C, 30 min
6: 98 percent / 80percent aq. AcOH / 7 h / 70 °C
With formic acid; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; toluene-4-sulfonic acid; hydrazine hydrate; acetic acid; dicyclohexyl-carbodiimide; In methanol; nitromethane; dichloromethane; ethyl acetate;
DOI:10.1039/p19960000985
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