Yttrium(III) trifluoromethanesulfonate

Base Information

• Chemical Name: Yttrium(III) trifluoromethanesulfonate
• CAS No.: 52093-30-8
• Molecular Formula: C3F9O9S3Y
• Molecular Weight: 536.11
• Hs Code.: 28469099
• European Community (EC) Number: 628-665-8
• DSSTox Substance ID: DTXSID20370050
• Nikkaji Number: J1.322.328I
• Mol file: 52093-30-8.mol

Synonyms:Yttrium(III) trifluoromethanesulfonate;52093-30-8;Yttrium triflate;MFCD00209623;trifluoromethanesulfonate;yttrium(3+);Trifluoromethanesulfonic acid yttrium(III) salt;yttrium(iii)trifluoromethanesulfonate;YTTRIUM TRIFLUOROMETHANESULFONATE;Yttrium(III) Triflate;C3F9O9S3Y;AMY9063;DTXSID20370050;Yttrium trifluoromethanesulfonate?;JPJIEXKLJOWQQK-UHFFFAOYSA-K;AKOS015852988;Yttrium tris(trifluoromethanesulfonate);GS-6839;SC10887;SY011731;CS-0019215;FT-0696564;T1921;yttrium(3+) ion tritrifluoromethanesulfonate;O12159;A828921;J-525167;Yttrium(III) triflate, Trace metals grade, 99.99%;TRIFLUOROMETHANESULFONIC ACID YTTRIUM(III) SALT;YTTRIUM (III) TRIFLUOROMETHANESULPHONATE;YTTRIUM TRIFLATE;YTTRIUM(III) TRIFLATE;YTTRIUM(III) TRIFLUOROMETHANESULFONATE

Chemical Property of Yttrium(III) trifluoromethanesulfonate

Chemical Property:

• Appearance/Colour: white crystalline powder
• Refractive Index: ">
• Boiling Point: 162 °C at 760 mmHg
• PSA: 196.74000
• Density: 1.7
• LogP: 3.39660
• Storage Temp.: Inert atmosphere,Room Temperature
• Water Solubility.: Soluble in water
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 18
• Rotatable Bond Count: 0
• Exact Mass: 535.761912
• Heavy Atom Count: 25
• Complexity: 145

Purity/Quality:

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

Yttrium(III) trifluoromethanesulfonate ^*data from reagent suppliers

Safty Information:

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

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].[Y+3]
• Uses: Yttrium(III) trifluoromethanesulfonate is a lewis acid catalyst used in the conversion of enantioenriched N-?acyloxazolidinones to chiral esters, amides, and acids. Recently used to promote glycosidation of glycosyl fluorides and as a catalyst in the preparation of pyridine and quinoline derivatives.