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bis[3-(octadecyloxy)propyl] [3-({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yI]methyl}amino)propyl]phosphonate

Base Information Edit
  • Chemical Name:bis[3-(octadecyloxy)propyl] [3-({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yI]methyl}amino)propyl]phosphonate
  • CAS No.:1404216-68-7
  • Molecular Formula:C59H105N4O6P
  • Molecular Weight:997.48
  • Hs Code.:
  • Mol file:1404216-68-7.mol
bis[3-(octadecyloxy)propyl] [3-({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yI]methyl}amino)propyl]phosphonate

Synonyms:bis[3-(octadecyloxy)propyl] [3-({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yI]methyl}amino)propyl]phosphonate

Suppliers and Price of bis[3-(octadecyloxy)propyl] [3-({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yI]methyl}amino)propyl]phosphonate
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Chemical Property of bis[3-(octadecyloxy)propyl] [3-({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yI]methyl}amino)propyl]phosphonate Edit
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Technology Process of bis[3-(octadecyloxy)propyl] [3-({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yI]methyl}amino)propyl]phosphonate

There total 3 articles about bis[3-(octadecyloxy)propyl] [3-({[4-(benzyloxy)-5H-pyrrolo[3,2-d]pyrimidin-7-yI]methyl}amino)propyl]phosphonate 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:
4-benzyloxy-5H-pyrrolo[3,2-d]pyrimidine-7-carbaldehyde; bis[3-(octadecyloxy)propyl] (3-aminopropyl)phosphonate; With methanol; at 60 ℃; for 18h;
With sodium tetrahydroborate; at 30 ℃; for 0.5h;
Guidance literature:
Multi-step reaction with 2 steps
1.1: hydrogen; trifluoroacetic acid / palladium 10% on activated carbon / methanol / 40 °C / 760.05 Torr
2.1: methanol / 18 h / 60 °C
2.2: 0.5 h / 30 °C
With methanol; hydrogen; trifluoroacetic acid; palladium 10% on activated carbon; In methanol;
Guidance literature:
Multi-step reaction with 3 steps
1.1: oxalyl dichloride / dichloromethane; N,N-dimethyl-formamide / 3 h
1.2: 2 h
2.1: hydrogen; trifluoroacetic acid / palladium 10% on activated carbon / methanol / 40 °C / 760.05 Torr
3.1: methanol / 18 h / 60 °C
3.2: 0.5 h / 30 °C
With methanol; oxalyl dichloride; hydrogen; trifluoroacetic acid; palladium 10% on activated carbon; In methanol; dichloromethane; N,N-dimethyl-formamide;
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