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N-(17-azido-3,6,9,12,15-pentaoxaheptadec-1-yl)-N2-(1-methyl-ethyl)-N2-([2-(2,3,6,7,12,13,16,17-octahydro-1H,5H,11H,15H-pyrido[3,2,1-ij]quinolizino[1',9':6,7,8]chromeno[2,3-f]quinolin-4-ium-9-yl)phenyl]carbonyl)glycinamide chloride

Base Information
  • Chemical Name:N-(17-azido-3,6,9,12,15-pentaoxaheptadec-1-yl)-N2-(1-methyl-ethyl)-N2-([2-(2,3,6,7,12,13,16,17-octahydro-1H,5H,11H,15H-pyrido[3,2,1-ij]quinolizino[1',9':6,7,8]chromeno[2,3-f]quinolin-4-ium-9-yl)phenyl]carbonyl)glycinamide chloride
  • CAS No.:1356146-64-9
  • Molecular Formula:C49H64N7O8*Cl
  • Molecular Weight:914.542
  • Hs Code.:
N-(17-azido-3,6,9,12,15-pentaoxaheptadec-1-yl)-N<sub>2</sub>-(1-methyl-ethyl)-N<sub>2</sub>-([2-(2,3,6,7,12,13,16,17-octahydro-1H,5H,11H,15H-pyrido[3,2,1-ij]quinolizino[1',9':6,7,8]chromeno[2,3-f]quinolin-4-ium-9-yl)phenyl]carbonyl)glycinamide chloride

Synonyms:

Suppliers and Price of N-(17-azido-3,6,9,12,15-pentaoxaheptadec-1-yl)-N2-(1-methyl-ethyl)-N2-([2-(2,3,6,7,12,13,16,17-octahydro-1H,5H,11H,15H-pyrido[3,2,1-ij]quinolizino[1',9':6,7,8]chromeno[2,3-f]quinolin-4-ium-9-yl)phenyl]carbonyl)glycinamide chloride
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Chemical Property of N-(17-azido-3,6,9,12,15-pentaoxaheptadec-1-yl)-N2-(1-methyl-ethyl)-N2-([2-(2,3,6,7,12,13,16,17-octahydro-1H,5H,11H,15H-pyrido[3,2,1-ij]quinolizino[1',9':6,7,8]chromeno[2,3-f]quinolin-4-ium-9-yl)phenyl]carbonyl)glycinamide chloride
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Technology Process of N-(17-azido-3,6,9,12,15-pentaoxaheptadec-1-yl)-N2-(1-methyl-ethyl)-N2-([2-(2,3,6,7,12,13,16,17-octahydro-1H,5H,11H,15H-pyrido[3,2,1-ij]quinolizino[1',9':6,7,8]chromeno[2,3-f]quinolin-4-ium-9-yl)phenyl]carbonyl)glycinamide chloride

There total 6 articles about N-(17-azido-3,6,9,12,15-pentaoxaheptadec-1-yl)-N2-(1-methyl-ethyl)-N2-([2-(2,3,6,7,12,13,16,17-octahydro-1H,5H,11H,15H-pyrido[3,2,1-ij]quinolizino[1',9':6,7,8]chromeno[2,3-f]quinolin-4-ium-9-yl)phenyl]carbonyl)glycinamide chloride 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:
formaldehyd; isopropylamine; In toluene; at 20 ℃; for 2h;
1-azido-17-isocyano-3,6,9,12,15-pentaoxaheptadecane; rhodamine 101; With hydrogenchloride; In methanol; water; toluene; at 100 ℃; for 1h; Microwave irradiation;
DOI:10.1039/c1ob06581e
Guidance literature:
Multi-step reaction with 6 steps
1.1: tetrahydrofuran / 4 h / 0 - 20 °C
2.1: sodium azide; sodium hydrogencarbonate / water / 12 h / 80 °C
3.1: phosphoric acid; triphenylphosphine / diethyl ether / 24 h / 0 - 20 °C
3.2: 24 h / 0 °C
4.1: 3 h / Reflux
5.1: diisopropylamine; trichlorophosphate / dichloromethane / 2 h / 0 - 20 °C
6.1: toluene / 2 h / 20 °C
6.2: 1 h / 100 °C / Microwave irradiation
With sodium azide; phosphoric acid; sodium hydrogencarbonate; diisopropylamine; triphenylphosphine; trichlorophosphate; In tetrahydrofuran; diethyl ether; dichloromethane; water; toluene; 3.1: Staudinger reaction / 6.2: Ugi condensation;
DOI:10.1039/c1ob06581e
Guidance literature:
Multi-step reaction with 4 steps
1.1: phosphoric acid; triphenylphosphine / diethyl ether / 24 h / 0 - 20 °C
1.2: 24 h / 0 °C
2.1: 3 h / Reflux
3.1: diisopropylamine; trichlorophosphate / dichloromethane / 2 h / 0 - 20 °C
4.1: toluene / 2 h / 20 °C
4.2: 1 h / 100 °C / Microwave irradiation
With phosphoric acid; diisopropylamine; triphenylphosphine; trichlorophosphate; In diethyl ether; dichloromethane; toluene; 1.1: Staudinger reaction / 4.2: Ugi condensation;
DOI:10.1039/c1ob06581e
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