Potassium trifluoromethanesulphinate

Base Information

• Chemical Name: Potassium trifluoromethanesulphinate
• CAS No.: 41804-89-1
• Molecular Formula: CH F3 O2 S . K
• Molecular Weight: 172.169
• Hs Code.: 2930909090
• European Community (EC) Number: 255-556-9
• DSSTox Substance ID: DTXSID50194620
• Nikkaji Number: J278.279K
• Mol file: 41804-89-1.mol

Synonyms:Potassium trifluoromethanesulphinate;41804-89-1;potassium trifluoromethanesulfinate;potassium;trifluoromethanesulfinate;EINECS 255-556-9;METHANESULFINIC ACID,1,1,1-TRIFLUORO-, POTASSIUM SALT (1:1);CF3KO2S;CHF3O2S.K;SCHEMBL1224663;C-H-F3-O2-S.K;potassium trifluoromethylsulfinate;SCHEMBL16009874;DTXSID50194620;BJOCFTZMSXIQNX-UHFFFAOYSA-N;MFCD00054650;AKOS025310404;Trifluoromethanesulfinic acid potassium salt;Trifluoromethanesulphinic Acid, Potassium Salt;Z56831342

Chemical Property of Potassium trifluoromethanesulphinate

Chemical Property:

• Vapor Pressure: 0.0369mmHg at 25°C
• Melting Point: 236-241 °C
• Boiling Point: 222.8 °C at 760 mmHg
• Flash Point: 88.5 °C
• PSA: 59.34000
• Density: g/cm³
• LogP: 1.25100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 0
• Exact Mass: 171.92081638
• Heavy Atom Count: 8
• Complexity: 89.8

Purity/Quality:

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

PotassiumTrifluoromethanesulfinate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38-38-37-36
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(F)(F)(F)S(=O)[O-].[K+]
• Uses: Potassium Trifluoromethanesulfinate is used in preparation of trifluoromethanesulfonyl compounds.

Technology Process of Potassium trifluoromethanesulphinate

There total 11 articles about Potassium trifluoromethanesulphinate 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: 96.0%

trifluoromethanesulfinic acid (34642-42-7) → potassium triflinate (41804-89-1)

Guidance literature:

With potassium carbonate; In ethanol; stoich. amts. of educts in abs. ethanol;

DOI:10.1016/S0022-1139(00)83984-6

Reference yield: 94.0%

Trifluoromethanesulfonyl fluoride (335-05-7) → potassium triflinate (41804-89-1)

Guidance literature:

With potassium sulfite; In methanol; water;

Reference yield: 91.0%

N-phenacylphenyl trifluoromethanesulfonamide → potassium triflinate (41804-89-1)

Guidance literature:

With potassium carbonate; In acetone; at 20 ℃; for 48h;

DOI:10.1002/chem.201204014

upstream raw materials:

1,3-Diphenyl-3-trifluoromethanesulfonyl-propan-1-one

benzyl trifluoromethyl sulfone

ethyl bromoacetate

Trifluoromethanesulfonyl fluoride

Downstream raw materials:

benzyl trifluoromethyl sulfone

(2-(trifluoromethylsulfonyl)ethyl)benzene

((E)-3-Trifluoromethanesulfonyl-allyl)-benzene

1-phenyl-2-((trifluoromethyl)sulfonyl)ethan-1-one