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C33H54O8S2Si

Base Information
  • Chemical Name:C33H54O8S2Si
  • CAS No.:1392829-19-4
  • Molecular Formula:C33H54O8S2Si
  • Molecular Weight:671.004
  • Hs Code.:
C<sub>33</sub>H<sub>54</sub>O<sub>8</sub>S<sub>2</sub>Si

Synonyms:C33H54O8S2Si

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Chemical Property of C33H54O8S2Si
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Technology Process of C33H54O8S2Si

There total 16 articles about C33H54O8S2Si 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:
Guidance literature:
With pyridine; Dess-Martin periodane; In dichloromethane; at 0 - 20 ℃;
DOI:10.1016/j.tetlet.2012.06.005
Guidance literature:
Multi-step reaction with 10 steps
1.1: boron trifluoride diethyl etherate / diethyl ether / 0 °C
2.1: sodium periodate; ruthenium trichloride; water; zinc(II) chloride / ethyl acetate; acetonitrile / 0 °C
3.1: toluene-4-sulfonic acid / tetrahydrofuran / 40 °C
4.1: sodium tetrahydroborate / methanol; dichloromethane / 0 °C
5.1: sodium hydride / tetrahydrofuran / 0 °C
5.2: 0 - 20 °C
6.1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / benzene / 80 °C
7.1: LiDBB / tetrahydrofuran / -78 °C
8.1: sulfur trioxide pyridine complex; dimethyl sulfoxide; triethylamine / dichloromethane / 0 - 20 °C
9.1: n-butyllithium / tetrahydrofuran / 20 °C
9.2: -78 - 0 °C
10.1: pyridine; Dess-Martin periodane / dichloromethane / 0 - 20 °C
With pyridine; ruthenium trichloride; sodium tetrahydroborate; sodium periodate; n-butyllithium; 2,2'-azobis(isobutyronitrile); boron trifluoride diethyl etherate; water; tri-n-butyl-tin hydride; sulfur trioxide pyridine complex; sodium hydride; Dess-Martin periodane; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine; zinc(II) chloride; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; ethyl acetate; acetonitrile; benzene; 6.1: Barton-McCombie deoxygenation / 8.1: Parikh-Doering oxidation;
DOI:10.1016/j.tetlet.2012.06.005
Guidance literature:
Multi-step reaction with 7 steps
1.1: sodium tetrahydroborate / methanol; dichloromethane / 0 °C
2.1: sodium hydride / tetrahydrofuran / 0 °C
2.2: 0 - 20 °C
3.1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / benzene / 80 °C
4.1: LiDBB / tetrahydrofuran / -78 °C
5.1: sulfur trioxide pyridine complex; dimethyl sulfoxide; triethylamine / dichloromethane / 0 - 20 °C
6.1: n-butyllithium / tetrahydrofuran / 20 °C
6.2: -78 - 0 °C
7.1: pyridine; Dess-Martin periodane / dichloromethane / 0 - 20 °C
With pyridine; sodium tetrahydroborate; n-butyllithium; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; sulfur trioxide pyridine complex; sodium hydride; Dess-Martin periodane; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; methanol; dichloromethane; benzene; 3.1: Barton-McCombie deoxygenation / 5.1: Parikh-Doering oxidation;
DOI:10.1016/j.tetlet.2012.06.005
upstream raw materials:

(2-furyl)methyl alcohol

C20H30O4Si

C21H32O5Si

C21H34O7Si

Downstream raw materials:

C33H56O8S2Si

C30H50O9Si

C30H52O9Si

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