C₃₀H₃₆N₂O₃

Base Information

Chemical Name:C₃₀H₃₆N₂O₃
CAS No.:1447825-82-2
Molecular Formula:C₃₀H₃₆N₂O₃
Molecular Weight:472.627
Hs Code.:

C<sub>30</sub>H<sub>36</sub>N<sub>2</sub>O<sub>3</sub>

Synonyms:

Suppliers and Price of C₃₀H₃₆N₂O₃

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 C₃₀H₃₆N₂O₃

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₀H₃₆N₂O₃

There total 11 articles about C₃₀H₃₆N₂O₃ 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:

: C₁₉H₃₀N₂O₂

: 2243-83-6
2-naphthaloyl chloride

: 1447825-82-2
C₃₀H₃₆N₂O₃

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 2h;
DOI:10.1021/jm400542h

Reference yield:

: C₂₇H₃₉NO₂SSi

: 1447825-82-2
C₃₀H₃₆N₂O₃

Guidance literature:: Multi-step reaction with 9 steps

1: dichloromethane; tetrahydrofuran / 0.67 h / 20 °C

2: hydrogenchloride / methanol; ethyl acetate / 5 h / 20 °C

3: sodium carbonate / tetrahydrofuran; water / 12 h / 20 °C

4: Dess-Martin periodane / dichloromethane / 0.5 h / 20 °C

5: 2-methyl-but-2-ene; sodium dihydrogenphosphate dihydrate; sodium chlorite / tetrahydrofuran; tert-butyl alcohol; water / 14 h / 20 °C

6: triethylamine; diphenyl phosphoryl azide / dichloromethane / 17.33 h / 0 - 20 °C

7: 29 h / Reflux

8: potassium carbonate / methanol / 14 h / 20 °C

9: triethylamine / dichloromethane / 2 h / 0 °C

With hydrogenchloride; sodium chlorite; sodium dihydrogenphosphate dihydrate; 2-methyl-but-2-ene; diphenyl phosphoryl azide; sodium carbonate; potassium carbonate; Dess-Martin periodane; triethylamine; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; tert-butyl alcohol; 1: |Grignard Reaction / 4: |Dess-Martin Oxidation;
DOI:10.1021/jm400542h

Reference yield:

: C₃₅H₄₉NO₂SSi

: 1447825-82-2
C₃₀H₃₆N₂O₃

Guidance literature:: Multi-step reaction with 8 steps

1: hydrogenchloride / methanol; ethyl acetate / 5 h / 20 °C

2: sodium carbonate / tetrahydrofuran; water / 12 h / 20 °C

3: Dess-Martin periodane / dichloromethane / 0.5 h / 20 °C

4: 2-methyl-but-2-ene; sodium dihydrogenphosphate dihydrate; sodium chlorite / tetrahydrofuran; tert-butyl alcohol; water / 14 h / 20 °C

5: triethylamine; diphenyl phosphoryl azide / dichloromethane / 17.33 h / 0 - 20 °C

6: 29 h / Reflux

7: potassium carbonate / methanol / 14 h / 20 °C

8: triethylamine / dichloromethane / 2 h / 0 °C

With hydrogenchloride; sodium chlorite; sodium dihydrogenphosphate dihydrate; 2-methyl-but-2-ene; diphenyl phosphoryl azide; sodium carbonate; potassium carbonate; Dess-Martin periodane; triethylamine; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; tert-butyl alcohol; 3: |Dess-Martin Oxidation;
DOI:10.1021/jm400542h