C₃₅H₅₀O₆Si

Base Information

Chemical Name:C₃₅H₅₀O₆Si
CAS No.:1334173-65-7
Molecular Formula:C₃₅H₅₀O₆Si
Molecular Weight:594.864
Hs Code.:

C<sub>35</sub>H<sub>50</sub>O<sub>6</sub>Si

Synonyms:C₃₅H₅₀O₆Si

Suppliers and Price of C₃₅H₅₀O₆Si

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 C₃₅H₅₀O₆Si

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₅H₅₀O₆Si

There total 11 articles about C₃₅H₅₀O₆Si 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: 89.0%

: 1334173-64-6
C₄₁H₅₆O₇SSi

: 1334173-65-7
C₃₅H₅₀O₆Si

Guidance literature:: With sodium hydrogencarbonate; In 1,2-dichloro-benzene; at 170 ℃; for 10h; Inert atmosphere;
DOI:10.1002/anie.201103550

Reference yield:

: 1334173-57-7
C₂₅H₃₀O₃Si

: 1334173-65-7
C₃₅H₅₀O₆Si

Guidance literature:: Multi-step reaction with 7 steps

1.1: N,N,N,N,N,N-hexamethylphosphoric triamide; lithium hexamethyldisilazane / tetrahydrofuran / -78 - 0 °C / Inert atmosphere

1.2: 13 h / -78 °C / Inert atmosphere

2.1: lithium borohydride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

3.1: dicobalt octacarbonyl / toluene / 1.5 h / 20 °C / Inert atmosphere

3.2: 12 h / 100 °C

4.1: tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine / dichloromethane / 15 h / 20 °C / Inert atmosphere

5.1: borane-THF; (3aR)-1-methyl-3,3-diphenyl-tetrahydro-pyrrolo[1,2-c][1,3,2]oxazaborole / tetrahydrofuran / 2 h / 20 °C / Inert atmosphere

6.1: sodium hydride / tetrahydrofuran; mineral oil / 0 - 20 °C / Inert atmosphere

6.2: 0 - 20 °C / Inert atmosphere

7.1: sodium hydrogencarbonate / 1,2-dichloro-benzene / 10 h / 170 °C / Inert atmosphere

With N,N,N,N,N,N-hexamethylphosphoric triamide; lithium borohydride; dicobalt octacarbonyl; borane-THF; tetra-(n-butyl)ammonium iodide; sodium hydride; sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; lithium hexamethyldisilazane; (3aR)-1-methyl-3,3-diphenyl-tetrahydro-pyrrolo[1,2-c][1,3,2]oxazaborole; In tetrahydrofuran; dichloromethane; 1,2-dichloro-benzene; toluene; mineral oil; 3.1: Pauson-Khand reaction / 3.2: Pauson-Khand reaction;
DOI:10.1002/anie.201103550

Reference yield:

: C₂₆H₃₄O₄Si

: 1334173-65-7
C₃₅H₅₀O₆Si

Guidance literature:: Multi-step reaction with 8 steps

1.1: pyridinium p-toluenesulfonate / isopropyl alcohol; toluene / 28 - 80 °C / Inert atmosphere

2.1: N,N,N,N,N,N-hexamethylphosphoric triamide; lithium hexamethyldisilazane / tetrahydrofuran / -78 - 0 °C / Inert atmosphere

2.2: 13 h / -78 °C / Inert atmosphere

3.1: lithium borohydride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

4.1: dicobalt octacarbonyl / toluene / 1.5 h / 20 °C / Inert atmosphere

4.2: 12 h / 100 °C

5.1: tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine / dichloromethane / 15 h / 20 °C / Inert atmosphere

6.1: borane-THF; (3aR)-1-methyl-3,3-diphenyl-tetrahydro-pyrrolo[1,2-c][1,3,2]oxazaborole / tetrahydrofuran / 2 h / 20 °C / Inert atmosphere

7.1: sodium hydride / tetrahydrofuran; mineral oil / 0 - 20 °C / Inert atmosphere

7.2: 0 - 20 °C / Inert atmosphere

8.1: sodium hydrogencarbonate / 1,2-dichloro-benzene / 10 h / 170 °C / Inert atmosphere

With N,N,N,N,N,N-hexamethylphosphoric triamide; lithium borohydride; dicobalt octacarbonyl; borane-THF; pyridinium p-toluenesulfonate; tetra-(n-butyl)ammonium iodide; sodium hydride; sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; lithium hexamethyldisilazane; (3aR)-1-methyl-3,3-diphenyl-tetrahydro-pyrrolo[1,2-c][1,3,2]oxazaborole; In tetrahydrofuran; dichloromethane; 1,2-dichloro-benzene; isopropyl alcohol; toluene; mineral oil; 4.1: Pauson-Khand reaction / 4.2: Pauson-Khand reaction;
DOI:10.1002/anie.201103550