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C25H36F2N2O4

Base Information
  • Chemical Name:C25H36F2N2O4
  • CAS No.:1292321-51-7
  • Molecular Formula:C25H36F2N2O4
  • Molecular Weight:466.569
  • Hs Code.:
C<sub>25</sub>H<sub>36</sub>F<sub>2</sub>N<sub>2</sub>O<sub>4</sub>

Synonyms:

Suppliers and Price of C25H36F2N2O4
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Chemical Property of C25H36F2N2O4
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Technology Process of C25H36F2N2O4

There total 13 articles about C25H36F2N2O4 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 water; lithium hydroxide; In tetrahydrofuran; methanol; at 75 ℃; for 3h;
DOI:10.1016/j.bmcl.2010.12.060
Guidance literature:
Multi-step reaction with 10 steps
1: n-butyllithium / tetrahydrofuran / -78 °C
2: sodium hexamethyldisilazane / tetrahydrofuran / -78 °C
3: hydrogenchloride / methanol / 20 °C
4: triethylamine / dichloromethane / 20 °C
5: dihydrogen peroxide; lithium hydroxide / tetrahydrofuran; water / 20 °C
6: diphenyl phosphoryl azide; N-ethyl-N,N-diisopropylamine / toluene / 100 °C
7: chloro-trimethyl-silane / dichloromethane / 20 °C
8: palladium 10% on activated carbon; hydrogen / ethanol
9: Decaborane / methanol / 20 °C
10: water; lithium hydroxide / tetrahydrofuran; methanol / 3 h / 75 °C
With hydrogenchloride; n-butyllithium; chloro-trimethyl-silane; Decaborane; diphenyl phosphoryl azide; palladium 10% on activated carbon; water; hydrogen; dihydrogen peroxide; sodium hexamethyldisilazane; triethylamine; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; toluene; 6: Curtius rearrangement;
DOI:10.1016/j.bmcl.2010.12.060
Guidance literature:
Multi-step reaction with 8 steps
1: hydrogenchloride / methanol / 20 °C
2: triethylamine / dichloromethane / 20 °C
3: dihydrogen peroxide; lithium hydroxide / tetrahydrofuran; water / 20 °C
4: diphenyl phosphoryl azide; N-ethyl-N,N-diisopropylamine / toluene / 100 °C
5: chloro-trimethyl-silane / dichloromethane / 20 °C
6: palladium 10% on activated carbon; hydrogen / ethanol
7: Decaborane / methanol / 20 °C
8: water; lithium hydroxide / tetrahydrofuran; methanol / 3 h / 75 °C
With hydrogenchloride; chloro-trimethyl-silane; Decaborane; diphenyl phosphoryl azide; palladium 10% on activated carbon; water; hydrogen; dihydrogen peroxide; triethylamine; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; toluene; 4: Curtius rearrangement;
DOI:10.1016/j.bmcl.2010.12.060
upstream raw materials:

C29H34F2N2O5

C22H23F2NO4

C18H26F2N2O2

C26H38F2N2O4

Downstream raw materials:

C25H37F2N3O3

C20H28F2N2O2

C20H29F2N3O

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