C₃₂H₃₅N₇O₈

Base Information

Chemical Name:C₃₂H₃₅N₇O₈
CAS No.:869883-72-7
Molecular Formula:C₃₂H₃₅N₇O₈
Molecular Weight:645.672
Hs Code.:

C<sub>32</sub>H<sub>35</sub>N<sub>7</sub>O<sub>8</sub>

Synonyms:C₃₂H₃₅N₇O₈

Suppliers and Price of C₃₂H₃₅N₇O₈

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of C₃₂H₃₅N₇O₈

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₂H₃₅N₇O₈

There total 9 articles about C₃₂H₃₅N₇O₈ 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: 68.0%

: 869883-71-6
C₂₁H₁₇N₅O₄

: 1-[(tert-butyloxycarbonylamino)-(tert-butyloxycarbonylimino)-methyl]-1H-pyrazole

: 869883-72-7
C₃₂H₃₅N₇O₈

Guidance literature:: In DMF (N,N-dimethyl-formamide); at 20 ℃; for 10h;

Reference yield:

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

: 869883-72-7
C₃₂H₃₅N₇O₈

Guidance literature:: Multi-step reaction with 9 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

8: methanol; hydrazine / 0.05 h / Heating / reflux

9: DMF (N,N-dimethyl-formamide) / 10 h / 20 °C

With methanol; di-isopropyl azodicarboxylate; tetra-(n-butyl)ammonium iodide; potassium carbonate; triethylamine; triphenylphosphine; hydrazine; 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

: 869883-72-7
C₃₂H₃₅N₇O₈

Guidance literature:: Multi-step reaction with 8 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

7: methanol; hydrazine / 0.05 h / Heating / reflux

8: DMF (N,N-dimethyl-formamide) / 10 h / 20 °C

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