N-methyl hexa(phenoxy)cyclotriphosphazenium trifluoromethanesulfonate

Base Information

• Chemical Name: N-methyl hexa(phenoxy)cyclotriphosphazenium trifluoromethanesulfonate
• CAS No.: 1356917-82-2
• Molecular Formula: CF₃O₃S*C₃₇H₃₃N₃O₆P₃
• Molecular Weight: 857.677
• Mol file: 1356917-82-2.mol

Synonyms:N-methyl hexa(phenoxy)cyclotriphosphazenium trifluoromethanesulfonate

Chemical Property of N-methyl hexa(phenoxy)cyclotriphosphazenium trifluoromethanesulfonate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of N-methyl hexa(phenoxy)cyclotriphosphazenium trifluoromethanesulfonate

There total 1 articles about N-methyl hexa(phenoxy)cyclotriphosphazenium trifluoromethanesulfonate 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: 93.0%

2,2,4,4,6,6-hexaphenoxycyclotriphosphazene (1184-10-7) + methyl trifluoromethanesulfonate (333-27-7) → N-methyl hexa(phenoxy)cyclotriphosphazenium trifluoromethanesulfonate (1356917-82-2)

Guidance literature:

In dichloromethane; at 25 ℃; for 24h; Inert atmosphere;

DOI:10.1021/ma202619j

Reference yield: 89.0%

N-methyl hexa(phenoxy)cyclotriphosphazenium trifluoromethanesulfonate (1356917-82-2) → 2,2,4,4,6,6-hexaphenoxycyclotriphosphazene (1184-10-7)

Guidance literature:

With sodium iodide; In dichloromethane; at 25 ℃; for 48h; Inert atmosphere;

DOI:10.1021/ma202619j

Reference yield:

N-methyl hexa(phenoxy)cyclotriphosphazenium trifluoromethanesulfonate (1356917-82-2) → BF4(1-)*C38H35N3O6P3(1+)

Guidance literature:

Multi-step reaction with 2 steps

1: sodium iodide / dichloromethane / 48 h / 25 °C / Inert atmosphere

2: dichloromethane / 48 h / 25 °C / Inert atmosphere

With sodium iodide; In dichloromethane;

DOI:10.1021/ma202619j

upstream raw materials:

2,2,4,4,6,6-hexaphenoxycyclotriphosphazene

methyl trifluoromethanesulfonate

Downstream raw materials:

2,2,4,4,6,6-hexaphenoxycyclotriphosphazene