C₅₆H₈₂O₁₀Si₂

Base Information

Chemical Name:C₅₆H₈₂O₁₀Si₂
CAS No.:1385034-02-5
Molecular Formula:C₅₆H₈₂O₁₀Si₂
Molecular Weight:971.432
Hs Code.:

C<sub>56</sub>H<sub>82</sub>O<sub>10</sub>Si<sub>2</sub>

Synonyms:C₅₆H₈₂O₁₀Si₂

Suppliers and Price of C₅₆H₈₂O₁₀Si₂

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 C₅₆H₈₂O₁₀Si₂

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₅₆H₈₂O₁₀Si₂

There total 6 articles about C₅₆H₈₂O₁₀Si₂ 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: 95.0%

: 1385033-99-7
C₅₇H₈₄O₉Si₂

: 1385034-02-5
C₅₆H₈₂O₁₀Si₂

Guidance literature:: With 2,6-dimethylpyridine; sodium periodate; osmium(VIII) oxide; In tetrahydrofuran; water; tert-butyl alcohol; at 22 ℃; for 3h;
DOI:10.1021/ol3015682

Reference yield:

: 870119-18-9
(2S)-3-[(tert-butyldiphenylsilyl)oxy]-2-(4-methoxybenzyloxy)propanal

: 1385034-02-5
C₅₆H₈₂O₁₀Si₂

Guidance literature:: Multi-step reaction with 4 steps

1.1: 2,6-di-tert-butyl-4-methylpyridine; (4R,5R)-2-bromo-1,3-bis[(4-methylphenyl)sulfonyl]-4,5-diphenyl-1,3,2-diazaborolidine / dichloromethane / 16 h / 0 - 22 °C / Inert atmosphere

1.2: 2 h / -78 °C / Inert atmosphere

2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 22 °C / Inert atmosphere

3.1: magnesium bromide ethyl etherate / dichloromethane / 0.08 h / -78 °C / Inert atmosphere

3.2: 12 h / -26 °C / Inert atmosphere

4.1: 2,6-dimethylpyridine; sodium periodate; osmium(VIII) oxide / tetrahydrofuran; water; tert-butyl alcohol / 3 h / 22 °C

With 2,6-dimethylpyridine; sodium periodate; osmium(VIII) oxide; 2,6-di-tert-butyl-4-methylpyridine; (4R,5R)-2-bromo-1,3-bis[(4-methylphenyl)sulfonyl]-4,5-diphenyl-1,3,2-diazaborolidine; magnesium bromide ethyl etherate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; water; tert-butyl alcohol;
DOI:10.1021/ol3015682

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 1385034-02-5
C₅₆H₈₂O₁₀Si₂

Guidance literature:: Multi-step reaction with 6 steps

1.1: 1H-imidazole / dichloromethane

2.1: methylenedimethyl sulfurane / tetrahydrofuran / -10 °C

3.1: 2,6-di-tert-butyl-4-methylpyridine; (4R,5R)-2-bromo-1,3-bis[(4-methylphenyl)sulfonyl]-4,5-diphenyl-1,3,2-diazaborolidine / dichloromethane / 16 h / 0 - 22 °C / Inert atmosphere

3.2: 2 h / -78 °C / Inert atmosphere

4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 22 °C / Inert atmosphere

5.1: magnesium bromide ethyl etherate / dichloromethane / 0.08 h / -78 °C / Inert atmosphere

5.2: 12 h / -26 °C / Inert atmosphere

6.1: 2,6-dimethylpyridine; sodium periodate; osmium(VIII) oxide / tetrahydrofuran; water; tert-butyl alcohol / 3 h / 22 °C

With 1H-imidazole; 2,6-dimethylpyridine; sodium periodate; osmium(VIII) oxide; 2,6-di-tert-butyl-4-methylpyridine; methylenedimethyl sulfurane; (4R,5R)-2-bromo-1,3-bis[(4-methylphenyl)sulfonyl]-4,5-diphenyl-1,3,2-diazaborolidine; magnesium bromide ethyl etherate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; water; tert-butyl alcohol;
DOI:10.1021/ol3015682