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2l5,4l5,6l5-1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6,6-hexaazido-

Base Information Edit
  • Chemical Name:2l5,4l5,6l5-1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6,6-hexaazido-
  • CAS No.:22295-99-4
  • Molecular Formula:N21P3
  • Molecular Weight:387.062
  • Hs Code.:
  • Mol file:22295-99-4.mol
2l5,4l5,6l5-1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6,6-hexaazido-

Synonyms:1,3,5,2,4,6-Triazatriphosphorine,2,2,4,4,6,6-hexaazido-2,2,4,4,6,6-hexahydro- (8CI,9CI)

Suppliers and Price of 2l5,4l5,6l5-1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6,6-hexaazido-
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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Total 2 raw suppliers
Chemical Property of 2l5,4l5,6l5-1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6,6-hexaazido- Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):
  • Hazard Codes: 3:;
     
  • Safety Statements:A violent explosive sensitive to shock or friction. Very unstable. Upon decompositi"> x and POx. See also AZIDES." target="_blank">A violent explosive sensitive to shock or friction. Very unstable. Upon decompositi 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 2l5,4l5,6l5-1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6,6-hexaazido-

There total 5 articles about 2l5,4l5,6l5-1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6,6-hexaazido- 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:
In acetone; addn. of activated NaN3 in 8 ml H2O to (PNCl2)3 in 6 ml acetone; short heating at 45°C; storing for 2 h;; addn. of 20 ml H2O; extraction with ether;;
Guidance literature:
In further solvent(s); P3N3Cl6 added to Schlenk flask under Ar; dissolved in propionitrile at room temp.; (CH3)3SiN3 added dropwise to stirred soln. under N2 purge; stream of N2 passed; soln. warmed to 60°C; stirred 3 h; the stirredfor 19 h at room temp.; react, mixt. concd. (30°C, 50 mbar); dried in vac.; purified by sublimation (0.001 mbar, 130°C oil bath, -86°C cold finger;
DOI:10.1002/anie.200601670
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