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C27H37FN2O4S

Base Information
  • Chemical Name:C27H37FN2O4S
  • CAS No.:1123173-71-6
  • Molecular Formula:C27H37FN2O4S
  • Molecular Weight:504.666
  • Hs Code.:
C<sub>27</sub>H<sub>37</sub>FN<sub>2</sub>O<sub>4</sub>S

Synonyms:

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Chemical Property of C27H37FN2O4S
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Technology Process of C27H37FN2O4S

There total 13 articles about C27H37FN2O4S 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 sodium tetrahydroborate; nickel(II) chloride hexahydrate; In methanol; at 0 - 5 ℃; for 2h; Inert atmosphere;
DOI:10.1021/jm300069y
Guidance literature:
Multi-step reaction with 4 steps
1.1: hydrogenchloride / 1,4-dioxane / 2 h / 25 °C / Inert atmosphere
2.1: sodium acetate / methanol; dichloromethane / 0.5 h / 25 °C / Inert atmosphere
2.2: 1 h / Inert atmosphere
2.3: 0.25 h / Inert atmosphere
3.1: potassium hydroxide / tetrahydrofuran / 0.33 h / Microwave irradiation
4.1: sodium tetrahydroborate; nickel(II) chloride hexahydrate / methanol / 2 h / 0 - 5 °C / Inert atmosphere
With hydrogenchloride; sodium tetrahydroborate; nickel(II) chloride hexahydrate; sodium acetate; potassium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane;
DOI:10.1021/jm300069y
Guidance literature:
Multi-step reaction with 12 steps
1.1: thionyl chloride / 0 - 25 °C / Inert atmosphere
2.1: diisobutylaluminium hydride / tetrahydrofuran; hexane / 4 h / 0 - 5 °C / Inert atmosphere
2.2: 0.5 h / 25 °C / Cooling with ice; Inert atmosphere
3.1: phosphorus tribromide / 24 h / 25 °C / Inert atmosphere
4.1: potassium carbonate / acetone / 2.5 h / 25 - 30 °C / Inert atmosphere
5.1: palladium diacetate; triethylamine; triphenylphosphine / tert-butyl methyl ether / 16 h / 25 °C / Inert atmosphere
6.1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / -70 °C / Inert atmosphere
7.1: Chiralpak AD-I / ethanol; n-heptane / Inert atmosphere
8.1: potassium peroxymonosulfate / tetrahydrofuran; water / 2 h / 40 °C / Inert atmosphere
9.1: hydrogenchloride / 1,4-dioxane / 2 h / 25 °C / Inert atmosphere
10.1: sodium acetate / methanol; dichloromethane / 0.5 h / 25 °C / Inert atmosphere
10.2: 1 h / Inert atmosphere
10.3: 0.25 h / Inert atmosphere
11.1: potassium hydroxide / tetrahydrofuran / 0.33 h / Microwave irradiation
12.1: sodium tetrahydroborate; nickel(II) chloride hexahydrate / methanol / 2 h / 0 - 5 °C / Inert atmosphere
With hydrogenchloride; sodium tetrahydroborate; lithium aluminium tetrahydride; thionyl chloride; potassium peroxymonosulfate; nickel(II) chloride hexahydrate; sodium acetate; palladium diacetate; phosphorus tribromide; diisobutylaluminium hydride; potassium carbonate; triethylamine; triphenylphosphine; potassium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; hexane; n-heptane; dichloromethane; tert-butyl methyl ether; water; acetone;
DOI:10.1021/jm300069y
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