Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

C25H44O5Si

Base Information Edit
  • Chemical Name:C25H44O5Si
  • CAS No.:947661-52-1
  • Molecular Formula:C25H44O5Si
  • Molecular Weight:452.707
  • Hs Code.:
  • Mol file:947661-52-1.mol
C<sub>25</sub>H<sub>44</sub>O<sub>5</sub>Si

Synonyms:C25H44O5Si

Suppliers and Price of C25H44O5Si
Supply Marketing:Edit
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 C25H44O5Si Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of C25H44O5Si

There total 15 articles about C25H44O5Si 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: 88.0%

Guidance literature:
With methanol; camphor-10-sulfonic acid; In dichloromethane; at 0 - 20 ℃; for 0.5h;
DOI:10.1016/j.tetlet.2007.05.021
Guidance literature:
Multi-step reaction with 14 steps
1.1: 82 percent / Zn; NaI / methanol / 4 h / Heating
2.1: 85 percent / N-bromosuccinimide / CH2Cl2 / 1 h / 0 - 20 °C
3.1: 86 percent / (n-Bu)3SnH; AIBN / benzene / 0.5 h / Heating
4.1: 83 percent / CrO3; aq. H2SO4 / acetone / 1 h / 0 - 20 °C
5.1: 82 percent / triphenylphosphine / tetrahydrofuran / 3 h / Heating
6.1: 80 percent / Li sand / tetrahydrofuran / 2 h / Heating
7.1: 84 percent / imidazole / CH2Cl2 / 12 h / 0 - 20 °C
8.1: n-BuLi; BF3*OEt2 / tetrahydrofuran / -78 °C
8.2: 88 percent / tetrahydrofuran / -78 °C
9.1: 77 percent / LiAlH4 / bis-(2-methoxy-ethyl) ether; tetrahydrofuran / 6 h / 155 °C
10.1: 82 percent / CSA / acetone / 1 h / 0 - 20 °C
11.1: 87 percent / Et3N; DMAP / CH2Cl2 / 12 h / 0 - 20 °C
12.1: 79 percent / AD-mix-β; CH3SO2NH2 / 2-methyl-propan-2-ol; H2O / 0 - 20 °C
13.1: 90 percent / 2,6-lutidine / CH2Cl2 / 0.5 h / 0 - 20 °C
14.1: 88 percent / methanol; CSA / CH2Cl2 / 0.5 h / 0 - 20 °C
With 1H-imidazole; 2,6-dimethylpyridine; chromium(VI) oxide; methanol; dmap; N-Bromosuccinimide; lithium aluminium tetrahydride; n-butyllithium; 2,2'-azobis(isobutyronitrile); methanesulfonamide; AD-mix-β; sulfuric acid; camphor-10-sulfonic acid; boron trifluoride diethyl etherate; tri-n-butyl-tin hydride; lithium; triethylamine; triphenylphosphine; sodium iodide; zinc; camphor-10-sulfonic acid; In tetrahydrofuran; methanol; dichloromethane; diethylene glycol dimethyl ether; water; acetone; tert-butyl alcohol; benzene; 4.1: Jones' oxidation;
DOI:10.1016/j.tetlet.2007.05.021
Guidance literature:
Multi-step reaction with 11 steps
1.1: 83 percent / CrO3; aq. H2SO4 / acetone / 1 h / 0 - 20 °C
2.1: 82 percent / triphenylphosphine / tetrahydrofuran / 3 h / Heating
3.1: 80 percent / Li sand / tetrahydrofuran / 2 h / Heating
4.1: 84 percent / imidazole / CH2Cl2 / 12 h / 0 - 20 °C
5.1: n-BuLi; BF3*OEt2 / tetrahydrofuran / -78 °C
5.2: 88 percent / tetrahydrofuran / -78 °C
6.1: 77 percent / LiAlH4 / bis-(2-methoxy-ethyl) ether; tetrahydrofuran / 6 h / 155 °C
7.1: 82 percent / CSA / acetone / 1 h / 0 - 20 °C
8.1: 87 percent / Et3N; DMAP / CH2Cl2 / 12 h / 0 - 20 °C
9.1: 79 percent / AD-mix-β; CH3SO2NH2 / 2-methyl-propan-2-ol; H2O / 0 - 20 °C
10.1: 90 percent / 2,6-lutidine / CH2Cl2 / 0.5 h / 0 - 20 °C
11.1: 88 percent / methanol; CSA / CH2Cl2 / 0.5 h / 0 - 20 °C
With 1H-imidazole; 2,6-dimethylpyridine; chromium(VI) oxide; methanol; dmap; lithium aluminium tetrahydride; n-butyllithium; methanesulfonamide; AD-mix-β; sulfuric acid; camphor-10-sulfonic acid; boron trifluoride diethyl etherate; lithium; triethylamine; triphenylphosphine; camphor-10-sulfonic acid; In tetrahydrofuran; dichloromethane; diethylene glycol dimethyl ether; water; acetone; tert-butyl alcohol; 1.1: Jones' oxidation;
DOI:10.1016/j.tetlet.2007.05.021
upstream raw materials:

C13H17O2I

C17H25O3Br

C16H20O2Cl2

C21H44O2Si2

Downstream raw materials:

C26H44O4Si

C32H58O4Si2

C32H58O5Si2

C50H86O8Si3

Post RFQ for Price