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4-Phenyl-2,6,7-trioxa-1-phosphabicyclo[2.2.2]octane1-oxide

Base Information
  • Chemical Name:4-Phenyl-2,6,7-trioxa-1-phosphabicyclo[2.2.2]octane1-oxide
  • CAS No.:2200-87-5
  • Molecular Formula:C10H11 O4 P
  • Molecular Weight:226.1657
  • Hs Code.:2902909090
  • Mol file:2200-87-5.mol
4-Phenyl-2,6,7-trioxa-1-phosphabicyclo[2.2.2]octane1-oxide

Synonyms:1,3-Propanediol,2-(hydroxymethyl)-2-phenyl-, cyclic phosphate (7CI,8CI)

Suppliers and Price of 4-Phenyl-2,6,7-trioxa-1-phosphabicyclo[2.2.2]octane1-oxide
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 4 raw suppliers
Chemical Property of 4-Phenyl-2,6,7-trioxa-1-phosphabicyclo[2.2.2]octane1-oxide
Chemical Property:
  • Vapor Pressure:0.000639mmHg at 25°C 
  • Boiling Point:319.3°Cat760mmHg 
  • Flash Point:160.7°C 
  • PSA:54.57000 
  • Density:1.38g/cm3 
  • LogP:2.10950 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 4-Phenyl-2,6,7-trioxa-1-phosphabicyclo[2.2.2]octane1-oxide

There total 5 articles about 4-Phenyl-2,6,7-trioxa-1-phosphabicyclo[2.2.2]octane1-oxide 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:
With dinitrogen tetraoxide; In chloroform; at 0 ℃;
Guidance literature:
Multi-step reaction with 3 steps
1: H2 / Pd-C / ethanol / 760 Torr / Ambient temperature
2: P(OEt)3
3: N2O4 / CHCl3 / 0 °C
With hydrogen; dinitrogen tetraoxide; triethyl phosphite; palladium on activated charcoal; In ethanol; chloroform;
Guidance literature:
Multi-step reaction with 4 steps
1: LiAlH4 / diethyl ether / 2 h / Heating
2: H2 / Pd-C / ethanol / 760 Torr / Ambient temperature
3: P(OEt)3
4: N2O4 / CHCl3 / 0 °C
With lithium aluminium tetrahydride; hydrogen; dinitrogen tetraoxide; triethyl phosphite; palladium on activated charcoal; In diethyl ether; ethanol; chloroform;
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