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C25H29F2N7O2

Base Information Edit
  • Chemical Name:C25H29F2N7O2
  • CAS No.:1459776-76-1
  • Molecular Formula:C25H29F2N7O2
  • Molecular Weight:497.548
  • Hs Code.:
  • Mol file:1459776-76-1.mol
C<sub>25</sub>H<sub>29</sub>F<sub>2</sub>N<sub>7</sub>O<sub>2</sub>

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Chemical Property of C25H29F2N7O2 Edit
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Technology Process of C25H29F2N7O2

There total 5 articles about C25H29F2N7O2 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:
p-Methoxybenzyl bromide; With sodium azide; In dimethyl sulfoxide; at 20 ℃; for 6h;
1-(1H-1,2,4-triazole-1-yl)-2-(2,4-difluorophenyl)-3-(N-propyl-N-propargylamino)-2-propanol; With copper(ll) sulfate pentahydrate; sodium L-ascorbate; In water; dimethyl sulfoxide; at 20 ℃; for 2h;
DOI:10.1039/c3ra41310a
Guidance literature:
Multi-step reaction with 4 steps
1.1: sodium hydroxide; cetyltrimethylammonim bromide / toluene / 3 h / 60 °C
1.2: 1 h / 0 °C
2.1: triethylamine / ethanol / 6 h / Reflux
3.1: potassium iodide; potassium carbonate / acetonitrile / 6 h / 20 °C
4.1: sodium azide / dimethyl sulfoxide / 6 h / 20 °C
4.2: 2 h / 20 °C
With sodium azide; cetyltrimethylammonim bromide; potassium carbonate; triethylamine; potassium iodide; sodium hydroxide; In ethanol; dimethyl sulfoxide; toluene; acetonitrile;
DOI:10.1039/c3ra41310a
Guidance literature:
Multi-step reaction with 3 steps
1.1: triethylamine / ethanol / 6 h / Reflux
2.1: potassium iodide; potassium carbonate / acetonitrile / 6 h / 20 °C
3.1: sodium azide / dimethyl sulfoxide / 6 h / 20 °C
3.2: 2 h / 20 °C
With sodium azide; potassium carbonate; triethylamine; potassium iodide; In ethanol; dimethyl sulfoxide; acetonitrile;
DOI:10.1039/c3ra41310a
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