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C44H56O2Si2

Base Information
  • Chemical Name:C44H56O2Si2
  • CAS No.:915315-62-7
  • Molecular Formula:C44H56O2Si2
  • Molecular Weight:673.098
  • Hs Code.:
C<sub>44</sub>H<sub>56</sub>O<sub>2</sub>Si<sub>2</sub>

Synonyms:C44H56O2Si2

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Chemical Property of C44H56O2Si2
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Technology Process of C44H56O2Si2

There total 11 articles about C44H56O2Si2 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:
Multi-step reaction with 2 steps
1.1: para-toluenesulfonic acid monohydrate / tetrahydrofuran / 1 h / Heating
2.1: lithium hydride / tetrahydrofuran; toluene / 65 h
2.2: N-bromosuccinimide; dibenzoylperoxide / CCl4 / 0.75 h
2.3: 15.0 g / potassium tert-butoxide; tetrabutyltinhydride; 2,2'-azobisisobutyronitrile / tetrahydrofuran / 77 h / Heating
With lithium hydride; toluene-4-sulfonic acid; In tetrahydrofuran; toluene;
DOI:10.1021/ol061962z
Guidance literature:
Multi-step reaction with 5 steps
1.1: ozone gas / CH2Cl2; methanol / 0.58 h / -78 °C
1.2: 15.0 g / sodium borohydride / CH2Cl2; methanol / 30 h / -15 °C
2.1: 31.0 g / 4-dimethylaminopyridine / dimethylformamide; various solvent(s) / 24 h / 20 °C
3.1: para-toluenesulfonic acid monohydrate / acetone; H2O / 3 h / Heating
4.1: para-toluenesulfonic acid monohydrate / tetrahydrofuran / 1 h / Heating
5.1: lithium hydride / tetrahydrofuran; toluene / 65 h
5.2: N-bromosuccinimide; dibenzoylperoxide / CCl4 / 0.75 h
5.3: 15.0 g / potassium tert-butoxide; tetrabutyltinhydride; 2,2'-azobisisobutyronitrile / tetrahydrofuran / 77 h / Heating
With dmap; lithium hydride; toluene-4-sulfonic acid; ozone; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; toluene;
DOI:10.1021/ol061962z
Guidance literature:
Multi-step reaction with 8 steps
1.1: diisobutylaluminum hydride / toluene / 2 h
2.1: hydrazine hydrate; hydrazine dihydrochloride / triethylene glycol / 1 h / 130 °C
3.1: 8.55 g / KOH / 220 °C
4.1: ozone gas / CH2Cl2; methanol / 0.58 h / -78 °C
4.2: 15.0 g / sodium borohydride / CH2Cl2; methanol / 30 h / -15 °C
5.1: 31.0 g / 4-dimethylaminopyridine / dimethylformamide; various solvent(s) / 24 h / 20 °C
6.1: para-toluenesulfonic acid monohydrate / acetone; H2O / 3 h / Heating
7.1: para-toluenesulfonic acid monohydrate / tetrahydrofuran / 1 h / Heating
8.1: lithium hydride / tetrahydrofuran; toluene / 65 h
8.2: N-bromosuccinimide; dibenzoylperoxide / CCl4 / 0.75 h
8.3: 15.0 g / potassium tert-butoxide; tetrabutyltinhydride; 2,2'-azobisisobutyronitrile / tetrahydrofuran / 77 h / Heating
With dmap; potassium hydroxide; hydrazine dihydrochloride; lithium hydride; diisobutylaluminium hydride; toluene-4-sulfonic acid; ozone; hydrazine hydrate; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; toluene; 2,2'-[1,2-ethanediylbis(oxy)]bisethanol;
DOI:10.1021/ol061962z
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