C₂₉H₁₉N₅O₆

Base Information

Chemical Name:C₂₉H₁₉N₅O₆
CAS No.:869883-70-5
Molecular Formula:C₂₉H₁₉N₅O₆
Molecular Weight:533.5
Hs Code.:

C<sub>29</sub>H<sub>19</sub>N<sub>5</sub>O<sub>6</sub>

Synonyms:C₂₉H₁₉N₅O₆

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₂₉H₁₉N₅O₆

Chemical Property:

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Technology Process of C₂₉H₁₉N₅O₆

There total 6 articles about C₂₉H₁₉N₅O₆ 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:

Reference yield:

: 33025-60-4
1-(3-hydroxy-1H-indol-1-yl)ethanone

: 869883-70-5
C₂₉H₁₉N₅O₆

Guidance literature:: Multi-step reaction with 7 steps

1: acetic acid / 5 h / Heating / reflux

2: triethylamine / methanol / 4 h / Heating / reflux

3: trichlorophosphate / 1.5 h / 10 - 60 °C

4: triethylamine / isopropyl alcohol / 2 h / Heating / reflux

5: ethylene glycol / 2 h / Heating / reflux

6: tetra-(n-butyl)ammonium iodide; potassium carbonate / DMF (N,N-dimethyl-formamide) / 48 h / 20 °C

7: di-isopropyl azodicarboxylate; triphenylphosphine / DMF (N,N-dimethyl-formamide) / 0 - 20 °C

With di-isopropyl azodicarboxylate; tetra-(n-butyl)ammonium iodide; potassium carbonate; triethylamine; triphenylphosphine; trichlorophosphate; In methanol; DMF (N,N-dimethyl-formamide); ethylene glycol; acetic acid; isopropyl alcohol; 4: Knoevenagel Condensation / 7: Mitsunobu reaction;

Reference yield:

: 100-01-6,104810-17-5
4-nitro-aniline

: 869883-70-5
C₂₉H₁₉N₅O₆

Guidance literature:: Multi-step reaction with 7 steps

1: acetic acid / 5 h / Heating / reflux

2: triethylamine / methanol / 4 h / Heating / reflux

3: trichlorophosphate / 1.5 h / 10 - 60 °C

4: triethylamine / isopropyl alcohol / 2 h / Heating / reflux

5: ethylene glycol / 2 h / Heating / reflux

6: tetra-(n-butyl)ammonium iodide; potassium carbonate / DMF (N,N-dimethyl-formamide) / 48 h / 20 °C

7: di-isopropyl azodicarboxylate; triphenylphosphine / DMF (N,N-dimethyl-formamide) / 0 - 20 °C

With di-isopropyl azodicarboxylate; tetra-(n-butyl)ammonium iodide; potassium carbonate; triethylamine; triphenylphosphine; trichlorophosphate; In methanol; DMF (N,N-dimethyl-formamide); ethylene glycol; acetic acid; isopropyl alcohol; 4: Knoevenagel Condensation / 7: Mitsunobu reaction;

Reference yield:

: 67766-00-1
N-acetyl-3-p-nitrophenylaminoindole

: 869883-70-5
C₂₉H₁₉N₅O₆

Guidance literature:: Multi-step reaction with 6 steps

1: triethylamine / methanol / 4 h / Heating / reflux

2: trichlorophosphate / 1.5 h / 10 - 60 °C

3: triethylamine / isopropyl alcohol / 2 h / Heating / reflux

4: ethylene glycol / 2 h / Heating / reflux

5: tetra-(n-butyl)ammonium iodide; potassium carbonate / DMF (N,N-dimethyl-formamide) / 48 h / 20 °C

6: di-isopropyl azodicarboxylate; triphenylphosphine / DMF (N,N-dimethyl-formamide) / 0 - 20 °C

With di-isopropyl azodicarboxylate; tetra-(n-butyl)ammonium iodide; potassium carbonate; triethylamine; triphenylphosphine; trichlorophosphate; In methanol; DMF (N,N-dimethyl-formamide); ethylene glycol; isopropyl alcohol; 3: Knoevenagel Condensation / 6: Mitsunobu reaction;