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(S)-N-(2-mercaptoethyl)-6-(3-(2-(methylamino)propyl)phenoxy)hexanamide tartrate

Base Information
  • Chemical Name:(S)-N-(2-mercaptoethyl)-6-(3-(2-(methylamino)propyl)phenoxy)hexanamide tartrate
  • CAS No.:1313762-78-5
  • Molecular Formula:C4H6O6*C18H30N2O2S
  • Molecular Weight:488.602
  • Hs Code.:
(S)-N-(2-mercaptoethyl)-6-(3-(2-(methylamino)propyl)phenoxy)hexanamide tartrate

Synonyms:(S)-N-(2-mercaptoethyl)-6-(3-(2-(methylamino)propyl)phenoxy)hexanamide tartrate

Suppliers and Price of (S)-N-(2-mercaptoethyl)-6-(3-(2-(methylamino)propyl)phenoxy)hexanamide tartrate
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Chemical Property of (S)-N-(2-mercaptoethyl)-6-(3-(2-(methylamino)propyl)phenoxy)hexanamide tartrate
Chemical Property:
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Technology Process of (S)-N-(2-mercaptoethyl)-6-(3-(2-(methylamino)propyl)phenoxy)hexanamide tartrate

There total 9 articles about (S)-N-(2-mercaptoethyl)-6-(3-(2-(methylamino)propyl)phenoxy)hexanamide tartrate 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:
(S)-6-((3-(2-methylamino)propyl)phenoxy)-N-(2-(tritylthio)ethyl)hexanamide; With mercury(II) diacetate; In ethanol; at 20 ℃; Cooling with ice;
With hydrogen sulfide; In ethanol; for 2h;
L-Tartaric acid; In ethanol; Inert atmosphere;
DOI:10.1021/jm2004943
Guidance literature:
Multi-step reaction with 2 steps
1.1: trifluoroacetic acid / dichloromethane / 0.25 h / 20 °C
2.1: mercury(II) diacetate / ethanol / 20 °C / Cooling with ice
2.2: 2 h
2.3: Inert atmosphere
With mercury(II) diacetate; trifluoroacetic acid; In ethanol; dichloromethane;
DOI:10.1021/jm2004943
Guidance literature:
Multi-step reaction with 5 steps
1.1: triethylamine / methanol / 0.5 h / Reflux
2.1: sodium hydride / hexanes; N,N-dimethyl-formamide / 16 h
3.1: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 8 h / Reflux
4.1: 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0 - 20 °C / Inert atmosphere
5.1: mercury(II) diacetate / ethanol / 20 °C / Cooling with ice
5.2: 2 h
5.3: Inert atmosphere
With 1-hydroxy-7-aza-benzotriazole; lithium hydroxide monohydrate; mercury(II) diacetate; water; sodium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; methanol; hexanes; ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm2004943
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