352439-37-3

  • Product Name:HO-PEG8- NH2
  • Molecular Formula:C16H35NO8
  • Purity:99%
  • Molecular Weight:369.451
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Product Details

Purity:99%

Hot Sale Chinese Factory Supply HO-PEG8- NH2 352439-37-3 In Stock

  • Molecular Formula:C16H35NO8
  • Molecular Weight:369.451
  • Boiling Point:464.4±40.0 °C(Predicted) 
  • PKA:14.36±0.10(Predicted) 
  • PSA:110.86000 
  • Density:1.091±0.06 g/cm3(Predicted) 
  • LogP:-0.24610 

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352439-37-3 Process route

α-(2-azidoethyl)-ω-hydroxyhexa(oxyethylene)
352439-36-2

α-(2-azidoethyl)-ω-hydroxyhexa(oxyethylene)

23-amino-3 ,6,9,12,15,18,21-heptaoxatricosan-1-ol
352439-37-3

23-amino-3 ,6,9,12,15,18,21-heptaoxatricosan-1-ol

Conditions
Conditions Yield
With triphenylphosphine; In tetrahydrofuran; at 20 ℃; for 10h; Inert atmosphere;
95%
α-(2-azidoethyl)-ω-hydroxyhexa(oxyethylene); With triphenylphosphine; In tetrahydrofuran; at 20 ℃; for 20h;
With water; In tetrahydrofuran; Further stages.;
90%
Tetraethylene glycol
112-60-7

Tetraethylene glycol

23-amino-3 ,6,9,12,15,18,21-heptaoxatricosan-1-ol
352439-37-3

23-amino-3 ,6,9,12,15,18,21-heptaoxatricosan-1-ol

Conditions
Conditions Yield
Multi-step reaction with 4 steps
1.1: pyridine
2.1: NaH / dimethylformamide / 0.5 h / 20 °C
2.2: dimethylformamide / 22 h / 20 °C
3.1: 0.51 g / p-TsOH / methanol
4.1: Ph3P / tetrahydrofuran / 20 h / 20 °C
4.2: 90 percent / H2O / tetrahydrofuran
With pyridine; sodium hydride; toluene-4-sulfonic acid; triphenylphosphine; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; 2.1: Williamson's ether synthesis / 4.1: Staudinger reduction reaction;
 
Multi-step reaction with 6 steps
1.1: 60 percent / Ag2O / CH2Cl2 / 48 h
2.1: 94 percent / sodium azide / dimethylformamide / 2.5 h / 110 °C
3.1: 92 percent / Et3N / CH2Cl2 / 0.83 h / 0 - 20 °C
4.1: NaH / dimethylformamide / 0.5 h / 20 °C
4.2: dimethylformamide / 22 h / 20 °C
5.1: 0.51 g / p-TsOH / methanol
6.1: Ph3P / tetrahydrofuran / 20 h / 20 °C
6.2: 90 percent / H2O / tetrahydrofuran
With sodium azide; sodium hydride; toluene-4-sulfonic acid; triethylamine; triphenylphosphine; silver(l) oxide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; 4.1: Williamson's ether synthesis / 6.1: Staudinger reduction reaction;
 
Multi-step reaction with 4 steps
1.1: N-ethyl-N,N-diisopropylamine; dmap; thionyl chloride / 0 °C
1.2: 0 °C
2.1: potassium iodide; silver(l) oxide / dichloromethane; water / 8 h / 0 - 5 °C
3.1: sodium azide / acetonitrile / 22 h / Inert atmosphere; Reflux
4.1: triphenylphosphine / tetrahydrofuran / 10 h / 20 °C / Inert atmosphere
With dmap; thionyl chloride; sodium azide; N-ethyl-N,N-diisopropylamine; triphenylphosphine; potassium iodide; silver(l) oxide; In tetrahydrofuran; dichloromethane; water; acetonitrile;
 

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