C₂₈H₃₃Cl₂N₃O₆

Base Information

Chemical Name:C₂₈H₃₃Cl₂N₃O₆
CAS No.:1424337-12-1
Molecular Formula:C₂₈H₃₃Cl₂N₃O₆
Molecular Weight:578.493
Hs Code.:

C<sub>28</sub>H<sub>33</sub>Cl<sub>2</sub>N<sub>3</sub>O<sub>6</sub>

Synonyms:C₂₈H₃₃Cl₂N₃O₆

Suppliers and Price of C₂₈H₃₃Cl₂N₃O₆

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 C₂₈H₃₃Cl₂N₃O₆

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₈H₃₃Cl₂N₃O₆

There total 15 articles about C₂₈H₃₃Cl₂N₃O₆ 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:

: C₃₁H₃₇Cl₂N₃O₆

: 1424337-12-1
C₂₈H₃₃Cl₂N₃O₆

Guidance literature:: With hydrogenchloride; In ethanol; water; at 20 ℃; for 12h;
DOI:10.1016/j.bmcl.2012.11.058

Reference yield:

: 629-03-8
1 ,6-dibromohexane

: 1424337-12-1
C₂₈H₃₃Cl₂N₃O₆

Guidance literature:: Multi-step reaction with 9 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 20 °C

2.1: potassium carbonate; potassium iodide / N,N-dimethyl-formamide / 19 h / 65 °C

3.1: sodium dihydrogenphosphate; sodium chlorite; dihydrogen peroxide / acetonitrile; water / 24.5 h / 15 - 20 °C

4.1: thionyl chloride / 6 h / Reflux

5.1: sodium hydride / tetrahydrofuran; mineral oil / 0.25 h / 20 °C

5.2: 1.5 h / 10 - 20 °C

6.1: hydrazine hydrate / ethanol / 2 h / Reflux

7.1: triethylamine / N,N-dimethyl-formamide / 24 h / 65 °C

8.1: ammonium fluoride / water; ethanol / 48 h / 45 °C

9.1: hydrogenchloride / water; ethanol / 12 h / 20 °C

With hydrogenchloride; ammonium fluoride; sodium chlorite; sodium dihydrogenphosphate; thionyl chloride; dihydrogen peroxide; sodium hydride; potassium carbonate; hydrazine hydrate; triethylamine; potassium iodide; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; acetonitrile; mineral oil;
DOI:10.1016/j.bmcl.2012.11.058

Reference yield:

: 24566-79-8
2-(6-bromohexyl)isoindole-1,3-dione

: 1424337-12-1
C₂₈H₃₃Cl₂N₃O₆

Guidance literature:: Multi-step reaction with 8 steps

1.1: potassium carbonate; potassium iodide / N,N-dimethyl-formamide / 19 h / 65 °C

2.1: sodium dihydrogenphosphate; sodium chlorite; dihydrogen peroxide / acetonitrile; water / 24.5 h / 15 - 20 °C

3.1: thionyl chloride / 6 h / Reflux

4.1: sodium hydride / tetrahydrofuran; mineral oil / 0.25 h / 20 °C

4.2: 1.5 h / 10 - 20 °C

5.1: hydrazine hydrate / ethanol / 2 h / Reflux

6.1: triethylamine / N,N-dimethyl-formamide / 24 h / 65 °C

7.1: ammonium fluoride / water; ethanol / 48 h / 45 °C

8.1: hydrogenchloride / water; ethanol / 12 h / 20 °C

With hydrogenchloride; ammonium fluoride; sodium chlorite; sodium dihydrogenphosphate; thionyl chloride; dihydrogen peroxide; sodium hydride; potassium carbonate; hydrazine hydrate; triethylamine; potassium iodide; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; acetonitrile; mineral oil;
DOI:10.1016/j.bmcl.2012.11.058