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C33H47BrO6Si

Base Information Edit
  • Chemical Name:C33H47BrO6Si
  • CAS No.:1315567-83-9
  • Molecular Formula:C33H47BrO6Si
  • Molecular Weight:647.722
  • Hs Code.:
  • Mol file:1315567-83-9.mol
C<sub>33</sub>H<sub>47</sub>BrO<sub>6</sub>Si

Synonyms:C33H47BrO6Si

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Chemical Property of C33H47BrO6Si Edit
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Technology Process of C33H47BrO6Si

There total 8 articles about C33H47BrO6Si 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 tetrabutyl ammonium fluoride; acetic acid; In tetrahydrofuran; at 0 ℃;
DOI:10.1038/nchem.1074
Guidance literature:
Multi-step reaction with 5 steps
1.1: 122 °C / neat (no solvent)
1.2: 20 °C
2.1: 1,2-dichloro-benzene / 250 °C / Microwave irradiation
3.1: iodine; magnesium / diethyl ether / 0 °C
4.1: pyridine; dibromo sulfoxide / diethyl ether / -40 °C
5.1: tetrabutyl ammonium fluoride; acetic acid / tetrahydrofuran / 0 °C
With pyridine; dibromo sulfoxide; tetrabutyl ammonium fluoride; iodine; magnesium; acetic acid; In tetrahydrofuran; diethyl ether; 1,2-dichloro-benzene; 1.1: Claisen rearrangement;
DOI:10.1038/nchem.1074
Guidance literature:
Multi-step reaction with 6 steps
1.1: isopropyl alcohol / 80 °C
2.1: 122 °C / neat (no solvent)
2.2: 20 °C
3.1: 1,2-dichloro-benzene / 250 °C / Microwave irradiation
4.1: iodine; magnesium / diethyl ether / 0 °C
5.1: pyridine; dibromo sulfoxide / diethyl ether / -40 °C
6.1: tetrabutyl ammonium fluoride; acetic acid / tetrahydrofuran / 0 °C
With pyridine; dibromo sulfoxide; tetrabutyl ammonium fluoride; iodine; magnesium; acetic acid; In tetrahydrofuran; diethyl ether; 1,2-dichloro-benzene; isopropyl alcohol; 2.1: Claisen rearrangement;
DOI:10.1038/nchem.1074
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