C₅₁H₈₂O₁₂SSi₃

Base Information

Chemical Name:C₅₁H₈₂O₁₂SSi₃
CAS No.:153145-46-1
Molecular Formula:C₅₁H₈₂O₁₂SSi₃
Molecular Weight:1003.53
Hs Code.:

C<sub>51</sub>H<sub>82</sub>O<sub>12</sub>SSi<sub>3</sub>

Synonyms:C₅₁H₈₂O₁₂SSi₃

Suppliers and Price of C₅₁H₈₂O₁₂SSi₃

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 C₅₁H₈₂O₁₂SSi₃

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₅₁H₈₂O₁₂SSi₃

There total 14 articles about C₅₁H₈₂O₁₂SSi₃ 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:

: 153145-26-7
C₃₂H₅₆O₇Si₂

: 153145-46-1
C₅₁H₈₂O₁₂SSi₃

Guidance literature:: Multi-step reaction with 7 steps

1: 92 percent / EtN(i-Pr)2, (Bu)4NI / CH₂Cl₂ / 32 h / Heating

2: 1.) LDA, 2.) mCPBA / 1.) THF, -78 deg C, 2.) hexane, 25 deg C, 5 h

3: 95 percent / CH₂Cl₂ / 15 h / -45 °C

4: 63 percent / Burgess' reagent

5: 80 percent / OsO₄, pyridine / diethyl ether / 12 h / 0 °C

6: Et₃N / -78 °C

7: LDA / 3 h / -35 °C

With pyridine; osmium(VIII) oxide; Burgess Reagent; tetra-(n-butyl)ammonium iodide; triethylamine; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; lithium diisopropyl amide; In diethyl ether; dichloromethane;

Reference yield:

: 153145-20-1
C₃₄H₅₈O₇Si₂

: 153145-46-1
C₅₁H₈₂O₁₂SSi₃

Guidance literature:: Multi-step reaction with 14 steps

1: O₃

2: KMnO₄, KH₂PO₄

4: 93 percent / LDA / tetrahydrofuran / 0.5 h / -78 °C

5: 100 percent / p-TsOH

6: 92 percent / PhSK / dimethylformamide / 3 h / 86 °C

7: acid

8: 92 percent / EtN(i-Pr)2, (Bu)4NI / CH₂Cl₂ / 32 h / Heating

9: 1.) LDA, 2.) mCPBA / 1.) THF, -78 deg C, 2.) hexane, 25 deg C, 5 h

10: 95 percent / CH₂Cl₂ / 15 h / -45 °C

11: 63 percent / Burgess' reagent

12: 80 percent / OsO₄, pyridine / diethyl ether / 12 h / 0 °C

13: Et₃N / -78 °C

14: LDA / 3 h / -35 °C

With pyridine; potassium permanganate; potassium dihydrogenphosphate; osmium(VIII) oxide; Burgess Reagent; tetra-(n-butyl)ammonium iodide; (2E)-3-(4-hydroxyphenyl-3-methoxyphenyl)-1-phenylprop-2-en-1-one; toluene-4-sulfonic acid; ozone; triethylamine; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 153145-25-6
C₃₆H₆₄O₈Si₂

: 153145-46-1
C₅₁H₈₂O₁₂SSi₃

Guidance literature:: Multi-step reaction with 8 steps

1: acid

2: 92 percent / EtN(i-Pr)2, (Bu)4NI / CH₂Cl₂ / 32 h / Heating

3: 1.) LDA, 2.) mCPBA / 1.) THF, -78 deg C, 2.) hexane, 25 deg C, 5 h

4: 95 percent / CH₂Cl₂ / 15 h / -45 °C

5: 63 percent / Burgess' reagent

6: 80 percent / OsO₄, pyridine / diethyl ether / 12 h / 0 °C

7: Et₃N / -78 °C

8: LDA / 3 h / -35 °C

With pyridine; osmium(VIII) oxide; Burgess Reagent; tetra-(n-butyl)ammonium iodide; triethylamine; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; lithium diisopropyl amide; In diethyl ether; dichloromethane;