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C30H58O4Si2

Base Information
  • Chemical Name:C30H58O4Si2
  • CAS No.:944052-11-3
  • Molecular Formula:C30H58O4Si2
  • Molecular Weight:538.959
  • Hs Code.:
C<sub>30</sub>H<sub>58</sub>O<sub>4</sub>Si<sub>2</sub>

Synonyms:C30H58O4Si2

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Chemical Property of C30H58O4Si2
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Technology Process of C30H58O4Si2

There total 11 articles about C30H58O4Si2 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; hydrogen fluoride; In tetrahydrofuran; at 0 - 20 ℃; for 5h;
DOI:10.1016/j.tetlet.2007.04.016
Guidance literature:
Multi-step reaction with 11 steps
1: 98 percent / CSA / CH2Cl2 / 0 - 20 °C
2: 78 percent / Li; liq. NH3 / tetrahydrofuran / 0.17 h / -33 °C
3: 70 percent / Et3N; DMAP / CH2Cl2 / 0 - 20 °C
4: 92 percent / TBAF / tetrahydrofuran / 0 - 20 °C
5: (COCl)2; DMSO; Et3N / CH2Cl2 / 2 h / -78 - 0 °C
6: CH2Cl2 / 20 °C
7: 86 percent / LiBH4 / tetrahydrofuran / 16 h / 0 - 20 °C
8: 96 percent / NaHMDS / tetrahydrofuran; dimethylformamide / 0 - 20 °C
9: 65 percent / TFA / 2-methyl-propan-2-ol / 2 h / 20 °C
10: 100 percent / 2,6-lutidine / 0.17 h / 0 °C
11: 75 percent / HF; pyridine / tetrahydrofuran / 5 h / 0 - 20 °C
With pyridine; 2,6-dimethylpyridine; dmap; lithium borohydride; oxalyl dichloride; camphor-10-sulfonic acid; hydrogen fluoride; tetrabutyl ammonium fluoride; ammonia; sodium hexamethyldisilazane; lithium; dimethyl sulfoxide; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; tert-butyl alcohol;
DOI:10.1016/j.tetlet.2007.04.016
Guidance literature:
Multi-step reaction with 10 steps
1: 78 percent / Li; liq. NH3 / tetrahydrofuran / 0.17 h / -33 °C
2: 70 percent / Et3N; DMAP / CH2Cl2 / 0 - 20 °C
3: 92 percent / TBAF / tetrahydrofuran / 0 - 20 °C
4: (COCl)2; DMSO; Et3N / CH2Cl2 / 2 h / -78 - 0 °C
5: CH2Cl2 / 20 °C
6: 86 percent / LiBH4 / tetrahydrofuran / 16 h / 0 - 20 °C
7: 96 percent / NaHMDS / tetrahydrofuran; dimethylformamide / 0 - 20 °C
8: 65 percent / TFA / 2-methyl-propan-2-ol / 2 h / 20 °C
9: 100 percent / 2,6-lutidine / 0.17 h / 0 °C
10: 75 percent / HF; pyridine / tetrahydrofuran / 5 h / 0 - 20 °C
With pyridine; 2,6-dimethylpyridine; dmap; lithium borohydride; oxalyl dichloride; hydrogen fluoride; tetrabutyl ammonium fluoride; ammonia; sodium hexamethyldisilazane; lithium; dimethyl sulfoxide; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; tert-butyl alcohol;
DOI:10.1016/j.tetlet.2007.04.016
upstream raw materials:

C36H72O4Si3

C35H48O4Si

C28H42O4Si

C47H56O4Si

Downstream raw materials:

C35H64O5Si2

C33H62O4Si2

C34H60O3Si2

C35H62O4Si2

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