C₂₈H₄₀Cl₂N₂O₄

Base Information

Chemical Name:C₂₈H₄₀Cl₂N₂O₄
CAS No.:956234-48-3
Molecular Formula:C₂₈H₄₀Cl₂N₂O₄
Molecular Weight:539.543
Hs Code.:

C<sub>28</sub>H<sub>40</sub>Cl<sub>2</sub>N<sub>2</sub>O<sub>4</sub>

Synonyms:C₂₈H₄₀Cl₂N₂O₄

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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 C₂₈H₄₀Cl₂N₂O₄

Chemical Property:

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Technology Process of C₂₈H₄₀Cl₂N₂O₄

There total 12 articles about C₂₈H₄₀Cl₂N₂O₄ 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:

: 956235-86-2
N-(2,6-dichlorobenzyl)-5-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-N,2,2,3,3-pentamethyl-4,14-dioxa-7-aza-3-silahexadecan-16-amine

: 956234-48-3
C₂₈H₄₀Cl₂N₂O₄

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 45 ℃; for 3h;

Reference yield:

: 629-03-8
1 ,6-dibromohexane

: 956234-48-3
C₂₈H₄₀Cl₂N₂O₄

Guidance literature:: Multi-step reaction with 8 steps

1: sodium hydroxide / tetrabutylammomium bromide / water / 5 h / 20 °C

2: cetyltributylphosphonium bromide / N,N-dimethyl-formamide / 3 h / 75 °C

3: hydrogen / palladium 10% on activated carbon / methanol / 2 h / 20 °C / 2070.21 Torr

4: triethylamine / dichloromethane / 20 °C

5: N-ethyl-N,N-diisopropylamine / 16 h / 45 °C

6: hydrazine / ethanol / 72 h / 20 °C

7: potassium carbonate / 1,4-dioxane / 16 h / 105 °C

8: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / 45 °C

With sodium hydroxide; tetrabutyl ammonium fluoride; hydrogen; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; hydrazine; palladium 10% on activated carbon; tetrabutylammomium bromide; cetyltributylphosphonium bromide; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 503068-31-3
[({2-[(6-bromohexyl)oxy]ethyl}oxy)methyl]benzene

: 956234-48-3
C₂₈H₄₀Cl₂N₂O₄

Guidance literature:: Multi-step reaction with 7 steps

1: cetyltributylphosphonium bromide / N,N-dimethyl-formamide / 3 h / 75 °C

2: hydrogen / palladium 10% on activated carbon / methanol / 2 h / 20 °C / 2070.21 Torr

3: triethylamine / dichloromethane / 20 °C

4: N-ethyl-N,N-diisopropylamine / 16 h / 45 °C

5: hydrazine / ethanol / 72 h / 20 °C

6: potassium carbonate / 1,4-dioxane / 16 h / 105 °C

7: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / 45 °C

With tetrabutyl ammonium fluoride; hydrogen; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; hydrazine; palladium 10% on activated carbon; cetyltributylphosphonium bromide; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;