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C29H25N9O

Base Information Edit
C<sub>29</sub>H<sub>25</sub>N<sub>9</sub>O

Synonyms:C29H25N9O

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Chemical Property of C29H25N9O Edit
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Technology Process of C29H25N9O

There total 15 articles about C29H25N9O 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 benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 2h;
Guidance literature:
Multi-step reaction with 11 steps
1: trichlorophosphate; N,N-dimethyl-aniline / 16 h / 0 - 60 °C
2: ammonium hydroxide / 2.5 h / 85 °C / Sealed tube
3: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 45 °C
4: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; sodium carbonate / 1,2-dimethoxyethane / 16 h / 100 °C
5: palladium 10% on activated carbon; hydrogen / ethyl acetate / 16 h / 45 °C
6: N-iodo-succinimide / dichloromethane; acetonitrile / 1.5 h / 20 °C
7: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium carbonate / water; 1,4-dioxane / 15 h / 100 °C
8: N-Bromosuccinimide / dichloromethane; acetonitrile / 0.5 h / 20 °C
9: tetrakis(triphenylphosphine) palladium(0) / 1,4-dioxane; acetonitrile / 1 h / 125 °C / Inert atmosphere; Sealed tube; Microwave irradiation
10: trifluoroacetic acid / water / 48 h
11: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 2 h / 20 °C
With ammonium hydroxide; N-Bromosuccinimide; N-iodo-succinimide; tetrakis(triphenylphosphine) palladium(0); dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; palladium 10% on activated carbon; hydrogen; sodium carbonate; potassium carbonate; benzotriazol-1-ol; N,N-dimethyl-aniline; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; trichlorophosphate; In 1,4-dioxane; 1,2-dimethoxyethane; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; acetonitrile;
Guidance literature:
Multi-step reaction with 9 steps
1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; 1,1'-bis-(diphenylphosphino)ferrocene; potassium acetate / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere
2: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; sodium carbonate / 1,2-dimethoxyethane / 16 h / 100 °C
3: palladium 10% on activated carbon; hydrogen / ethyl acetate / 16 h / 45 °C
4: N-iodo-succinimide / dichloromethane; acetonitrile / 1.5 h / 20 °C
5: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium carbonate / water; 1,4-dioxane / 15 h / 100 °C
6: N-Bromosuccinimide / dichloromethane; acetonitrile / 0.5 h / 20 °C
7: tetrakis(triphenylphosphine) palladium(0) / 1,4-dioxane; acetonitrile / 1 h / 125 °C / Inert atmosphere; Sealed tube; Microwave irradiation
8: trifluoroacetic acid / water / 48 h
9: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 2 h / 20 °C
With 1,1'-bis-(diphenylphosphino)ferrocene; N-Bromosuccinimide; N-iodo-succinimide; tetrakis(triphenylphosphine) palladium(0); dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; palladium 10% on activated carbon; hydrogen; potassium acetate; sodium carbonate; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In 1,4-dioxane; 1,2-dimethoxyethane; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; acetonitrile;
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