1,2,4,3,5-Trithia(4-SIV)diazole, 1-[[(trifluoromethyl)sulfonyl]imino]-1,1-dihydro-

Base Information

• Chemical Name: 1,2,4,3,5-Trithia(4-SIV)diazole, 1-[[(trifluoromethyl)sulfonyl]imino]-1,1-dihydro-
• CAS No.: 58355-86-5
• Molecular Formula: CF3N3O2S4
• Molecular Weight: 271.2848
• Mol file: 58355-86-5.mol

Synonyms:1,2,4,3,5-Trithia(4-s(iv))diazole, 1-(((trifluoromethyl)sulfonyl)imino)-1,1-dihydro-;58355-86-5;1,2,4,3,5-Trithia(4-SIV)diazole, 1-[[(trifluoromethyl)sulfonyl]imino]-1,1-dihydro-

Chemical Property of 1,2,4,3,5-Trithia(4-SIV)diazole, 1-[[(trifluoromethyl)sulfonyl]imino]-1,1-dihydro-

Chemical Property:

• Vapor Pressure: 0.001mmHg at 25°C
• Boiling Point: 310°Cat760mmHg
• Flash Point: 141.3°C
• Density: 2.47g/cm³
• XLogP3: 4.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 11
• Rotatable Bond Count: 1
• Exact Mass: 270.88254543
• Heavy Atom Count: 13
• Complexity: 395

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(F)(F)(F)S(=O)(=O)N=S1N=S=NS1
• Isomeric SMILES: C(F)(F)(F)S(=O)(=O)/N=S\1/N=S=NS1

Technology Process of 1,2,4,3,5-Trithia(4-SIV)diazole, 1-[[(trifluoromethyl)sulfonyl]imino]-1,1-dihydro-

There total 6 articles about 1,2,4,3,5-Trithia(4-SIV)diazole, 1-[[(trifluoromethyl)sulfonyl]imino]-1,1-dihydro- 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: 42.0%

S3N2Cl2 + Trifluoromethanesulfonamide (421-85-2) → 1-trifluoromethylsulfonylimino-1.lambda,2,4λ,3,5-trithiadiazole (58355-86-5)

Guidance literature:

In tetrachloromethane; refluxing in CCl4 5 h; extn. with CH2Cl2;

Reference yield:

trifluoromethylsulfonic anhydride (358-23-6) + tetrasulfur tetranitride (28950-34-7) → 1-trifluoromethylsulfonylimino-1.lambda,2,4λ,3,5-trithiadiazole (58355-86-5)

Guidance literature:

In dichloromethane; in dry atmosphere, in anhyrd. CH2Cl2, at reflux temp., 3 h, a mixture formation; removal of solvent in vac. and subliming the residue yields S3N2N(CF3SO2);

Reference yield:

Trifluoromethanesulfonamide (421-85-2) → 1-trifluoromethylsulfonylimino-1.lambda,2,4λ,3,5-trithiadiazole (58355-86-5)

Guidance literature:

With 1-chloro-1λ⁴,2,4λ⁴,3,5-trithiadiazolium chloride;

upstream raw materials:

Trifluoromethanesulfonamide

trifluoro-methanesulfonyl isocyanate

trifluoromethylsulfonic anhydride

tetrasulfur tetranitride