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C36H44ClFN2O5

Base Information
  • Chemical Name:C36H44ClFN2O5
  • CAS No.:1335557-68-0
  • Molecular Formula:C36H44ClFN2O5
  • Molecular Weight:639.207
  • Hs Code.:
C<sub>36</sub>H<sub>44</sub>ClFN<sub>2</sub>O<sub>5</sub>

Synonyms:C36H44ClFN2O5

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Chemical Property of C36H44ClFN2O5
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Technology Process of C36H44ClFN2O5

There total 11 articles about C36H44ClFN2O5 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 dmap; methanesulfonyl chloride; triethylamine; In dichloromethane; at 20 ℃; for 1h;
Guidance literature:
Multi-step reaction with 10 steps
1.1: oxalyl dichloride / dichloromethane; N,N-dimethyl-formamide / 1 h / 25 °C
1.2: 12 h / 25 °C
2.1: boron tribromide / dichloromethane / 1.5 h / -78 - 25 °C
3.1: nitric acid; tetrabutylammomium bromide / water; 1,2-dichloro-ethane / 19 h / 20 - 26 °C
4.1: potassium carbonate; potassium iodide / acetone / 20 - 56 °C
5.1: water; sodium dithionite / tetrahydrofuran / 10 - 20.4 °C
6.1: dmap; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C
7.1: diisopropylamine; n-butyllithium / hexane; tetrahydrofuran / 0.58 h / -78 °C
7.2: 0.5 h / -78 °C
7.3: -78 - 20 °C
8.1: acetic acid; sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 1 h / 20 °C
9.1: tetra-(n-butyl)ammonium iodide; sodium hydrogencarbonate / acetonitrile / 24 h / 70 °C
10.1: dmap; triethylamine; methanesulfonyl chloride / dichloromethane / 1 h / 20 °C
With dmap; n-butyllithium; sodium dithionite; oxalyl dichloride; tetrabutylammomium bromide; water; nitric acid; boron tribromide; tetra-(n-butyl)ammonium iodide; sodium tris(acetoxy)borohydride; sodium hydrogencarbonate; potassium carbonate; acetic acid; methanesulfonyl chloride; triethylamine; diisopropylamine; N-ethyl-N,N-diisopropylamine; potassium iodide; In tetrahydrofuran; hexane; dichloromethane; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide; acetone; acetonitrile;
Guidance literature:
Multi-step reaction with 11 steps
1.1: N,N,N,N,-tetramethylethylenediamine; sec.-butyllithium / tetrahydrofuran / 2 h / -78 °C
1.2: 2 h / -78 - 25 °C
2.1: oxalyl dichloride / dichloromethane; N,N-dimethyl-formamide / 1 h / 25 °C
2.2: 12 h / 25 °C
3.1: boron tribromide / dichloromethane / 1.5 h / -78 - 25 °C
4.1: nitric acid; tetrabutylammomium bromide / water; 1,2-dichloro-ethane / 19 h / 20 - 26 °C
5.1: potassium carbonate; potassium iodide / acetone / 20 - 56 °C
6.1: water; sodium dithionite / tetrahydrofuran / 10 - 20.4 °C
7.1: dmap; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C
8.1: diisopropylamine; n-butyllithium / hexane; tetrahydrofuran / 0.58 h / -78 °C
8.2: 0.5 h / -78 °C
8.3: -78 - 20 °C
9.1: acetic acid; sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 1 h / 20 °C
10.1: tetra-(n-butyl)ammonium iodide; sodium hydrogencarbonate / acetonitrile / 24 h / 70 °C
11.1: dmap; triethylamine; methanesulfonyl chloride / dichloromethane / 1 h / 20 °C
With dmap; n-butyllithium; sodium dithionite; oxalyl dichloride; N,N,N,N,-tetramethylethylenediamine; tetrabutylammomium bromide; water; sec.-butyllithium; nitric acid; boron tribromide; tetra-(n-butyl)ammonium iodide; sodium tris(acetoxy)borohydride; sodium hydrogencarbonate; potassium carbonate; acetic acid; methanesulfonyl chloride; triethylamine; diisopropylamine; N-ethyl-N,N-diisopropylamine; potassium iodide; In tetrahydrofuran; hexane; dichloromethane; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide; acetone; acetonitrile;
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