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DIBENZYL DIETHYLPHOSPHORAMIDITE

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DIBENZYL DIETHYLPHOSPHORAMIDITE Basic information

Product Name:
DIBENZYL DIETHYLPHOSPHORAMIDITE
Synonyms:
  • Bis(benzyloxy)(diethylaMino)phosphine
  • Dibenzyl (DiethylaMido)phosphite
  • DibenzyloxydiethylaMinophosphine
  • N,N-Diethyl-phosphoraMidous Acid Bis(phenylMethyl) Ester
  • DIBENZYL DIETHYLPHOSPHORAMIDITE
  • DIBENZYL N,N-DIETHYLPHOSPHORAMIDITE
  • DIBENZYL-N,N-DIETHYLPHOSPHOROAMIDITE
  • DIBENZYL DIETHYLPHOSPHORAMIDITE, TECH., 85%
CAS:
67746-43-4
MF:
C18H24NO2P
MW:
317.36
Product Categories:
  • Phospholipids - 13C & 2H
  • Regant series
  • Phosphorylating and Phosphitylating Agents
  • OLED materials,pharm chemical,electronic
Mol File:
67746-43-4.mol
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DIBENZYL DIETHYLPHOSPHORAMIDITE Chemical Properties

Boiling point:
131-132 °C(Press: 0.0001 Torr)
Density 
1.06 g/mL at 25 °C(lit.)
vapor pressure 
0.71 psi ( 55 °C)
refractive index 
n20/D 1.545(lit.)
Flash point:
95 °F
storage temp. 
2-8°C
solubility 
Soluble in chloroform.
pka
4.01±0.70(Predicted)
form 
Oil
color 
Clear Colourless to Pale Yellow
Sensitive 
Moisture Sensitive
BRN 
4189915
Stability:
Light Sensitive
CAS DataBase Reference
67746-43-4
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Safety Information

Hazard Codes 
Xi
Risk Statements 
10-36/37/38
Safety Statements 
16-26-37/39
RIDADR 
UN 1993 3/PG 3
WGK Germany 
3
10-21
HazardClass 
3.2
PackingGroup 
III

MSDS

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DIBENZYL DIETHYLPHOSPHORAMIDITE Usage And Synthesis

Chemical Properties

Clear Colourless Liquid

Uses

Dibenzyl N,N-diethylphosphoramidite may be used:

  • as phosphitylating reagent in the synthesis of glycosyl phosphites and phosphates
  • for phosphorylating the alcohols
  • in the preparation of 6-dibenzylphosphate-1,3,5-tri-O-PMB-myo-inositol

Uses

Dibenzyl diethylphosphoramidite is a useful reagent for the efficient phosphorylative conversion of alcohols into their corresponding dibenzylphosphorotriesters as well as dibenzyl glycosyl phosphites, which can easily be converted to glycosyl phosphates or used in glycosylation reagents in oligosaccharide synthesis.

General Description

Dibenzyl N,N-diethylphosphoramidite is repoted to be suitable reagent for the efficient 1H-tetrazole-catalyzed ′phosphite-triester′ phosphorylation of the protected serine derivatives.

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