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C36H54F2N8O

Base Information Edit
C<sub>36</sub>H<sub>54</sub>F<sub>2</sub>N<sub>8</sub>O

Synonyms:C36H54F2N8O

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Chemical Property of C36H54F2N8O Edit
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Technology Process of C36H54F2N8O

There total 14 articles about C36H54F2N8O 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 tris(acetoxy)borohydride; acetic acid; In dichloromethane; at 20 ℃; for 3h; Inert atmosphere;
DOI:10.1021/ml400370w
Guidance literature:
Multi-step reaction with 13 steps
1: sodium; propan-1-ol / toluene / 12 h / Reflux; Inert atmosphere
2: tetrahydrofuran / 72 h / 20 °C / Inert atmosphere
3: hydrogenchloride / methanol; 1,4-dioxane / 2 h / 20 °C / Inert atmosphere
4: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; triethylamine / N,N-dimethyl-formamide / 20 °C / Inert atmosphere
5: phosphorus pentachloride / dichloromethane / 2 h / 0 - 20 °C / Inert atmosphere
6: dichloromethane; tert-Amyl alcohol / 0 - 20 °C / Inert atmosphere
7: acetic acid / ethyl acetate / 0.5 h / 80 °C / Inert atmosphere
8: palladium 10% on activated carbon; hydrogen / methanol / 20 °C / 2585.81 Torr / Inert atmosphere
9: hydrogen bromide / 2 h / 100 °C / Inert atmosphere
10: sodium hydroxide / water; dichloromethane / 20 °C / pH 12 / Inert atmosphere
11: sodium azide / ethanol / 4 h / 100 °C / Inert atmosphere
12: hydrogenchloride / 1,4-dioxane / 3 h / 20 °C / Inert atmosphere
13: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 3 h / 20 °C / Inert atmosphere
With hydrogenchloride; propan-1-ol; sodium azide; phosphorus pentachloride; palladium 10% on activated carbon; hydrogen bromide; hydrogen; sodium; sodium tris(acetoxy)borohydride; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; tert-Amyl alcohol; ethanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; toluene;
DOI:10.1021/ml400370w
Guidance literature:
Multi-step reaction with 12 steps
1: tetrahydrofuran / 72 h / 20 °C / Inert atmosphere
2: hydrogenchloride / methanol; 1,4-dioxane / 2 h / 20 °C / Inert atmosphere
3: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; triethylamine / N,N-dimethyl-formamide / 20 °C / Inert atmosphere
4: phosphorus pentachloride / dichloromethane / 2 h / 0 - 20 °C / Inert atmosphere
5: dichloromethane; tert-Amyl alcohol / 0 - 20 °C / Inert atmosphere
6: acetic acid / ethyl acetate / 0.5 h / 80 °C / Inert atmosphere
7: palladium 10% on activated carbon; hydrogen / methanol / 20 °C / 2585.81 Torr / Inert atmosphere
8: hydrogen bromide / 2 h / 100 °C / Inert atmosphere
9: sodium hydroxide / water; dichloromethane / 20 °C / pH 12 / Inert atmosphere
10: sodium azide / ethanol / 4 h / 100 °C / Inert atmosphere
11: hydrogenchloride / 1,4-dioxane / 3 h / 20 °C / Inert atmosphere
12: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 3 h / 20 °C / Inert atmosphere
With hydrogenchloride; sodium azide; phosphorus pentachloride; palladium 10% on activated carbon; hydrogen bromide; hydrogen; sodium tris(acetoxy)borohydride; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; tert-Amyl alcohol; ethanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/ml400370w
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