1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6-pentafluoro-2,2,4,4,6,6-hexahydro-6-phenoxy-

Base Information

• Chemical Name: 1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6-pentafluoro-2,2,4,4,6,6-hexahydro-6-phenoxy-
• CAS No.: 33027-68-8
• Molecular Formula: C6H5F5N3OP3
• Molecular Weight: 323.038
• Mol file: 33027-68-8.mol

Synonyms:2,2,4,4,6-Pentafluoro-6-phenoxy-2λ5,4λ5,6λ5-[1,3,5,2,4,6]triazatriphosphinine;Phenyloxypentafluorcyclotriphosphazen;

Chemical Property of 1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6-pentafluoro-2,2,4,4,6,6-hexahydro-6-phenoxy-

Chemical Property:

• Refractive Index: 1.4300 to 1.4340
• Boiling Point: 46 °C (0.8 mmHg)
• PKA: -24.59±0.39(Predicted)
• PSA: 75.74000
• Density: 1.91±0.1 g/cm3(Predicted)
• LogP: 5.07190

Purity/Quality:

98%,99%, ^*data from raw suppliers

Pentafluoro(phenoxy)cyclotriphosphazene ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6-pentafluoro-2,2,4,4,6,6-hexahydro-6-phenoxy-

There total 3 articles about 1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6-pentafluoro-2,2,4,4,6,6-hexahydro-6-phenoxy- 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:

Reference yield: 72.4%

phenol (108-95-2,27073-41-2) → pentafluoro(phenoxy)cyclotriphosphazene (33027-68-8)

Guidance literature:

With hexafluorophosphazene; diethylamine; at -30 ℃; for 1h; Reagent/catalyst;

Reference yield:

pentachloride phenoxy cyclotriphosphazene (3028-10-2) → pentafluoro(phenoxy)cyclotriphosphazene (33027-68-8)

Guidance literature:

With sodium fluoride; In acetonitrile; at 80 ℃; for 5h;

Reference yield:

sodium phenoxide (139-02-6) → pentafluoro(phenoxy)cyclotriphosphazene (33027-68-8)

Guidance literature:

With hexafluorophosphazene; In diethyl ether;

upstream raw materials:

sodium phenoxide

pentachloride phenoxy cyclotriphosphazene

phenol

Refernces

• 1、 -. "Preparation method of pentafluoro aromatic oxyl cyclotriphosphazene". Paragraph 0016-0017; 0022-0023; 0024; 0025-0026. . Retrieved 2018/03/25.