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O6-((3-((2-(2-(2-(2,2,2-trifluoroacetamido)ethoxy)ethoxy)ethoxy)methyl))benzyl)guanine

Base Information Edit
  • Chemical Name:O6-((3-((2-(2-(2-(2,2,2-trifluoroacetamido)ethoxy)ethoxy)ethoxy)methyl))benzyl)guanine
  • CAS No.:1370437-59-4
  • Molecular Formula:C21H25F3N6O5
  • Molecular Weight:498.462
  • Hs Code.:
  • Mol file:1370437-59-4.mol
O<sub>6</sub>-((3-((2-(2-(2-(2,2,2-trifluoroacetamido)ethoxy)ethoxy)ethoxy)methyl))benzyl)guanine

Synonyms:O6-((3-((2-(2-(2-(2,2,2-trifluoroacetamido)ethoxy)ethoxy)ethoxy)methyl))benzyl)guanine

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Chemical Property of O6-((3-((2-(2-(2-(2,2,2-trifluoroacetamido)ethoxy)ethoxy)ethoxy)methyl))benzyl)guanine Edit
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Technology Process of O6-((3-((2-(2-(2-(2,2,2-trifluoroacetamido)ethoxy)ethoxy)ethoxy)methyl))benzyl)guanine

There total 4 articles about O6-((3-((2-(2-(2-(2,2,2-trifluoroacetamido)ethoxy)ethoxy)ethoxy)methyl))benzyl)guanine 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:
(3-((2-(2-(2-(2,2,2-trifluoroacetamido)ethoxy)ethoxy)ethoxy)methyl))benzyl alcohol; With potassium tert-butylate; In N,N-dimethyl-formamide; at 0 ℃; for 0.0833333h;
1‐(2‐amino‐9H‐purin‐6‐yl)‐1‐methylpyrrolidin‐1‐ium chloride; In N,N-dimethyl-formamide; at 20 ℃; for 3h;
DOI:10.1039/c2ob25231g
Guidance literature:
Multi-step reaction with 4 steps
1.1: sodium hydride / tetrahydrofuran; mineral oil / 0.08 h / 0 °C
1.2: 3 h / 20 °C
2.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C / Reflux
3.1: triethylamine / ethanol / 5 h / 20 °C
4.1: potassium tert-butylate / N,N-dimethyl-formamide / 0.08 h / 0 °C
4.2: 3 h / 20 °C
With lithium aluminium tetrahydride; potassium tert-butylate; sodium hydride; triethylamine; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; mineral oil;
DOI:10.1039/c2ob25231g
Guidance literature:
Multi-step reaction with 3 steps
1.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C / Reflux
2.1: triethylamine / ethanol / 5 h / 20 °C
3.1: potassium tert-butylate / N,N-dimethyl-formamide / 0.08 h / 0 °C
3.2: 3 h / 20 °C
With lithium aluminium tetrahydride; potassium tert-butylate; triethylamine; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;
DOI:10.1039/c2ob25231g
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