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C25H22N2O5

Base Information
  • Chemical Name:C25H22N2O5
  • CAS No.:792948-31-3
  • Molecular Formula:C25H22N2O5
  • Molecular Weight:430.46
  • Hs Code.:
C<sub>25</sub>H<sub>22</sub>N<sub>2</sub>O<sub>5</sub>

Synonyms:C25H22N2O5

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Chemical Property of C25H22N2O5
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Technology Process of C25H22N2O5

There total 16 articles about C25H22N2O5 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:
Multi-step reaction with 11 steps
1: 93 mg / Et3N / CH2Cl2 / 12 h / 0 °C
2: Zn; AcOH / CH2Cl2 / 0.33 h / 20 °C
3: 451 mg / aq. HCl / tetrahydrofuran / 24 h / 20 °C
4: 91 percent / [1,3-Mes2-(N2C3H5)]Cl2(PCy3)Ru=CHPh / CH2Cl2 / 12 h / Heating
5: K2CO3 / methanol / 9 h / 0 °C
6: MnO2 / CH2Cl2 / 72 h / 20 °C
7: aq. NaClO2; KH2PO4; 2-methyl-2-butene / 2-methyl-propan-2-ol / 3 h / 20 °C
8: 11 mg / SOCl2 / 18 h / 20 °C
9: RuCl3*3H2O / 110 °C
10: CF3CO2H; BF3*Et2O / 0.17 h / 20 °C
11: 9 mg / TsOH / 40 h / 100 °C
With hydrogenchloride; manganese(IV) oxide; ruthenium trichloride; sodium chlorite; potassium dihydrogenphosphate; thionyl chloride; 2-methyl-but-2-ene; [1,3-Mes2-(N2C3H5)]Cl2(PCy3)Ru=CHPh; boron trifluoride diethyl etherate; potassium carbonate; toluene-4-sulfonic acid; acetic acid; triethylamine; trifluoroacetic acid; zinc; In tetrahydrofuran; methanol; dichloromethane; tert-butyl alcohol;
DOI:10.1016/j.tet.2004.07.040
Guidance literature:
Multi-step reaction with 16 steps
1: 100 percent / aq. KHCO3 / ethyl acetate / 14 h / 0 °C
2: 100 percent / aq. NaIO4 / methanol / 4 h / 0 °C
3: 37 percent / xylene / 60 h / 140 °C
4: 76 percent / (PCy3)2Cl2Ru=CHPh / CH2Cl2 / 24 h / 20 °C
5: TMSCl; NaI / acetonitrile / 10 h / 20 °C
6: 93 mg / Et3N / CH2Cl2 / 12 h / 0 °C
7: Zn; AcOH / CH2Cl2 / 0.33 h / 20 °C
8: 451 mg / aq. HCl / tetrahydrofuran / 24 h / 20 °C
9: 91 percent / [1,3-Mes2-(N2C3H5)]Cl2(PCy3)Ru=CHPh / CH2Cl2 / 12 h / Heating
10: K2CO3 / methanol / 9 h / 0 °C
11: MnO2 / CH2Cl2 / 72 h / 20 °C
12: aq. NaClO2; KH2PO4; 2-methyl-2-butene / 2-methyl-propan-2-ol / 3 h / 20 °C
13: 11 mg / SOCl2 / 18 h / 20 °C
14: RuCl3*3H2O / 110 °C
15: CF3CO2H; BF3*Et2O / 0.17 h / 20 °C
16: 9 mg / TsOH / 40 h / 100 °C
With hydrogenchloride; manganese(IV) oxide; ruthenium trichloride; sodium chlorite; sodium periodate; potassium dihydrogenphosphate; Grubbs catalyst first generation; chloro-trimethyl-silane; thionyl chloride; 2-methyl-but-2-ene; [1,3-Mes2-(N2C3H5)]Cl2(PCy3)Ru=CHPh; boron trifluoride diethyl etherate; potassium carbonate; potassium hydrogencarbonate; toluene-4-sulfonic acid; acetic acid; triethylamine; trifluoroacetic acid; sodium iodide; zinc; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; acetonitrile; xylene; tert-butyl alcohol;
DOI:10.1016/j.tet.2004.07.040
Guidance literature:
Multi-step reaction with 12 steps
1: TMSCl; NaI / acetonitrile / 10 h / 20 °C
2: 93 mg / Et3N / CH2Cl2 / 12 h / 0 °C
3: Zn; AcOH / CH2Cl2 / 0.33 h / 20 °C
4: 451 mg / aq. HCl / tetrahydrofuran / 24 h / 20 °C
5: 91 percent / [1,3-Mes2-(N2C3H5)]Cl2(PCy3)Ru=CHPh / CH2Cl2 / 12 h / Heating
6: K2CO3 / methanol / 9 h / 0 °C
7: MnO2 / CH2Cl2 / 72 h / 20 °C
8: aq. NaClO2; KH2PO4; 2-methyl-2-butene / 2-methyl-propan-2-ol / 3 h / 20 °C
9: 11 mg / SOCl2 / 18 h / 20 °C
10: RuCl3*3H2O / 110 °C
11: CF3CO2H; BF3*Et2O / 0.17 h / 20 °C
12: 9 mg / TsOH / 40 h / 100 °C
With hydrogenchloride; manganese(IV) oxide; ruthenium trichloride; sodium chlorite; potassium dihydrogenphosphate; chloro-trimethyl-silane; thionyl chloride; 2-methyl-but-2-ene; [1,3-Mes2-(N2C3H5)]Cl2(PCy3)Ru=CHPh; boron trifluoride diethyl etherate; potassium carbonate; toluene-4-sulfonic acid; acetic acid; triethylamine; trifluoroacetic acid; sodium iodide; zinc; In tetrahydrofuran; methanol; dichloromethane; acetonitrile; tert-butyl alcohol;
DOI:10.1016/j.tet.2004.07.040
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