C₂₈H₄₃NO₄Si

Base Information

Chemical Name:C₂₈H₄₃NO₄Si
CAS No.:1438399-49-5
Molecular Formula:C₂₈H₄₃NO₄Si
Molecular Weight:485.739
Hs Code.:

C<sub>28</sub>H<sub>43</sub>NO<sub>4</sub>Si

Synonyms:

Suppliers and Price of C₂₈H₄₃NO₄Si

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 C₂₈H₄₃NO₄Si

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₈H₄₃NO₄Si

There total 3 articles about C₂₈H₄₃NO₄Si 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:

: 1438399-48-4
C₃₄H₅₇NO₄Si₂

: 1438399-49-5
C₂₈H₄₃NO₄Si

Guidance literature:: With camphor-10-sulfonic acid; In methanol; dichloromethane; at 0 ℃; for 6h;
DOI:10.1002/chem.201201332

Reference yield:

: 1195779-19-1
C₃₀H₄₃NO₄SSi

: 1438399-49-5
C₂₈H₄₃NO₄Si

Guidance literature:: Multi-step reaction with 6 steps

1.1: copper(l) iodide; methyllithium / tetrahydrofuran; diethyl ether / 8 h / 0 °C / Inert atmosphere

1.2: 0.5 h / 0 °C / Inert atmosphere

2.1: lithium triethylborohydride / tetrahydrofuran / 0.5 h / 0 - 25 °C / Inert atmosphere

3.1: [bis(acetoxy)iodo]benzene; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / dichloromethane / 0.5 h / 0 °C

4.1: dichloromethane / 12 h / 25 °C / Inert atmosphere

5.1: copper(l) iodide; methyllithium / tetrahydrofuran; diethyl ether / 8 h / 0 °C / Inert atmosphere

5.2: 0 °C / Inert atmosphere

6.1: camphor-10-sulfonic acid / methanol; dichloromethane / 6 h / 0 °C

With copper(l) iodide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene; camphor-10-sulfonic acid; methyllithium; lithium triethylborohydride; In tetrahydrofuran; methanol; diethyl ether; dichloromethane;
DOI:10.1002/chem.201201332

Reference yield:

: 1438399-44-0
C₃₇H₆₁NO₄SSi₂

: 1438399-49-5
C₂₈H₄₃NO₄Si

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium triethylborohydride / tetrahydrofuran / 0.5 h / 0 - 25 °C / Inert atmosphere

2.1: [bis(acetoxy)iodo]benzene; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / dichloromethane / 0.5 h / 0 °C

3.1: dichloromethane / 12 h / 25 °C / Inert atmosphere

4.1: copper(l) iodide; methyllithium / tetrahydrofuran; diethyl ether / 8 h / 0 °C / Inert atmosphere

4.2: 0 °C / Inert atmosphere

5.1: camphor-10-sulfonic acid / methanol; dichloromethane / 6 h / 0 °C

With copper(l) iodide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene; camphor-10-sulfonic acid; methyllithium; lithium triethylborohydride; In tetrahydrofuran; methanol; diethyl ether; dichloromethane;
DOI:10.1002/chem.201201332