C₂₆H₃₈O₆Si

Base Information

Chemical Name:C₂₆H₃₈O₆Si
CAS No.:1338989-63-1
Molecular Formula:C₂₆H₃₈O₆Si
Molecular Weight:474.67
Hs Code.:

C<sub>26</sub>H<sub>38</sub>O<sub>6</sub>Si

Synonyms:

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Chemical Property of C₂₆H₃₈O₆Si

Chemical Property:

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Technology Process of C₂₆H₃₈O₆Si

There total 12 articles about C₂₆H₃₈O₆Si 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:

: C₂₁H₃₂O₄Si

: 1338989-63-1
C₂₆H₃₈O₆Si

Guidance literature:: Multi-step reaction with 7 steps

1: zinc(II) tetrahydroborate / diethyl ether / -78 - -30 °C

2: tert.-butylhydroperoxide; bis(acetylacetonate)oxovanadium / dichloromethane / 0 - 24 °C

3: tetra-(n-butyl)ammonium iodide; sodium hydride / tetrahydrofuran / 0 - 24 °C

4: tetrabutyl ammonium fluoride / tetrahydrofuran / 25 °C

5: lithium aluminium tetrahydride / tetrahydrofuran / -15 °C

6: 2,6-dimethylpyridine / dichloromethane / -40 °C

7: methanol; potassium carbonate / -15 °C

With 2,6-dimethylpyridine; methanol; tert.-butylhydroperoxide; lithium aluminium tetrahydride; zinc(II) tetrahydroborate; bis(acetylacetonate)oxovanadium; tetrabutyl ammonium fluoride; tetra-(n-butyl)ammonium iodide; sodium hydride; potassium carbonate; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1016/j.tetlet.2011.08.051

Reference yield:

: C₁₁H₁₂O₄

: 1338989-63-1
C₂₆H₃₈O₆Si

Guidance literature:: Multi-step reaction with 9 steps

1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 25 °C

2: tert.-butyl lithium / tetrahydrofuran / -78 °C

3: zinc(II) tetrahydroborate / diethyl ether / -78 - -30 °C

4: tert.-butylhydroperoxide; bis(acetylacetonate)oxovanadium / dichloromethane / 0 - 24 °C

5: tetra-(n-butyl)ammonium iodide; sodium hydride / tetrahydrofuran / 0 - 24 °C

6: tetrabutyl ammonium fluoride / tetrahydrofuran / 25 °C

7: lithium aluminium tetrahydride / tetrahydrofuran / -15 °C

8: 2,6-dimethylpyridine / dichloromethane / -40 °C

9: methanol; potassium carbonate / -15 °C

With 2,6-dimethylpyridine; methanol; tert.-butylhydroperoxide; dmap; lithium aluminium tetrahydride; zinc(II) tetrahydroborate; bis(acetylacetonate)oxovanadium; tetrabutyl ammonium fluoride; tert.-butyl lithium; tetra-(n-butyl)ammonium iodide; sodium hydride; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1016/j.tetlet.2011.08.051

Reference yield:

: 1338989-56-2
C₂₉H₄₂O₆Si

: 1338989-63-1
C₂₆H₃₈O₆Si

Guidance literature:: Multi-step reaction with 4 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran / 25 °C

2: lithium aluminium tetrahydride / tetrahydrofuran / -15 °C

3: 2,6-dimethylpyridine / dichloromethane / -40 °C

4: methanol; potassium carbonate / -15 °C

With 2,6-dimethylpyridine; methanol; lithium aluminium tetrahydride; tetrabutyl ammonium fluoride; potassium carbonate; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.tetlet.2011.08.051