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C44H54N2O6SSi

Base Information
  • Chemical Name:C44H54N2O6SSi
  • CAS No.:1360744-12-2
  • Molecular Formula:C44H54N2O6SSi
  • Molecular Weight:767.074
  • Hs Code.:
C<sub>44</sub>H<sub>54</sub>N<sub>2</sub>O<sub>6</sub>SSi

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Chemical Property of C44H54N2O6SSi
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Technology Process of C44H54N2O6SSi

There total 11 articles about C44H54N2O6SSi 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 potassium tert-butylate; In tetrahydrofuran; at 0 ℃; for 1h;
DOI:10.1002/chem.201102101
Guidance literature:
Multi-step reaction with 9 steps
1.1: hydrogen iodide / water; toluene / 0.5 h / 0 - 20 °C
1.2: 2 h / Reflux
2.1: 1H-imidazole; dmap / dichloromethane / 24 h / 20 °C
3.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / N,N-dimethyl-formamide / 24 h / -78 - 20 °C
4.1: platinum(II) chloride / toluene / 1.45 h / 80 °C
5.1: dimethylsulfide borane complex / tetrahydrofuran / 0 - 20 °C
5.2: 1 h / 0 - 20 °C
6.1: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / 20 °C
6.2: 3 h / 20 °C
7.1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / toluene / Reflux
8.1: diisobutylaluminium hydride / dichloromethane; toluene / 0.5 h / -78 °C
9.1: potassium tert-butylate / tetrahydrofuran / 1 h / 0 °C
With 1H-imidazole; dmap; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; 2,2'-azobis(isobutyronitrile); dimethylsulfide borane complex; potassium tert-butylate; hydrogen iodide; tri-n-butyl-tin hydride; sodium hydride; diisobutylaluminium hydride; triethylamine; platinum(II) chloride; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; toluene; mineral oil; 3.1: Sonogashira coupling / 5.1: Hydroboration reaction / 7.1: Barton-McCombie deoxygenation / 9.1: Wittig reaction;
DOI:10.1002/chem.201102101
Guidance literature:
Multi-step reaction with 8 steps
1.1: 1H-imidazole; dmap / dichloromethane / 24 h / 20 °C
2.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / N,N-dimethyl-formamide / 24 h / -78 - 20 °C
3.1: platinum(II) chloride / toluene / 1.45 h / 80 °C
4.1: dimethylsulfide borane complex / tetrahydrofuran / 0 - 20 °C
4.2: 1 h / 0 - 20 °C
5.1: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / 20 °C
5.2: 3 h / 20 °C
6.1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / toluene / Reflux
7.1: diisobutylaluminium hydride / dichloromethane; toluene / 0.5 h / -78 °C
8.1: potassium tert-butylate / tetrahydrofuran / 1 h / 0 °C
With 1H-imidazole; dmap; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; 2,2'-azobis(isobutyronitrile); dimethylsulfide borane complex; potassium tert-butylate; tri-n-butyl-tin hydride; sodium hydride; diisobutylaluminium hydride; triethylamine; platinum(II) chloride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene; mineral oil; 2.1: Sonogashira coupling / 4.1: Hydroboration reaction / 6.1: Barton-McCombie deoxygenation / 8.1: Wittig reaction;
DOI:10.1002/chem.201102101
upstream raw materials:

C12H18O4

C7H9IO2

C12H17NO5

C21H26N2O6S

Downstream raw materials:

C28H32N2O4S

C27H30N2O5S

C29H36N2O5S

C27H32N2O5S

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