Neodymium(III) trifluoromethanesulfonate

Base Information

• Chemical Name: Neodymium(III) trifluoromethanesulfonate
• CAS No.: 34622-08-7
• Molecular Formula: C3F9NdO9S3
• Molecular Weight: 591.45
• Hs Code.: 28469099
• European Community (EC) Number: 627-624-1
• DSSTox Substance ID: DTXSID50370048
• Nikkaji Number: J1.021.250B
• Mol file: 34622-08-7.mol

Synonyms:Neodymium(III) trifluoromethanesulfonate;34622-08-7;MFCD00192343;neodymium(3+);trifluoromethanesulfonate;NEODYMIUM(III)TRIFLUOROMETHANESULFONATE;Neodymium(III) triflate;neodymium(3+),trifluoromethanesulfonate;Nd(OTf)3;DTXSID50370048;AMY37803;AKOS015852953;GS-6795;SC10983;SY016991;T1919;neodymium(3+) ion tritrifluoromethanesulfonate;H10826;Tris(trifluoromethylsulfonyloxy) neodymium(III);A874921;Trifluoromethanesulfonic Acid Neodymium(III) Salt;Neodymium(III) trifluoromethanesulfonate,98% (Neodymium triflate) Nd(CF3SO3)3

Chemical Property of Neodymium(III) trifluoromethanesulfonate

Chemical Property:

• Appearance/Colour: light purple crystalline powder
• Vapor Pressure: 1.14mmHg at 25°C
• Boiling Point: 162 °C at 760 mmHg
• PSA: 196.74000
• Density: 1.7 g/mL at 20 °C
• 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: 588.76380
• Heavy Atom Count: 25
• Complexity: 145

Purity/Quality:

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

Neodymium(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

Total 1 MSDS from other Authors

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-].[Nd+3]
• Uses: Neodymium(III) trifluoromethanesulfonate is used in the Aldol reaction of silyl enol ethers with aldehydes and as a catalyst for dehydration of fructose, Diels-Alder reactions of cyclopentadiene and alkyl acrylates, α-amination reactions of pyrazolones, polymerization reactions of cyclosiloxanes, direct polycondensation of dicarboxylic acids and diols, regioselective reductive ring opening of benzylidene acetals, Paal-Knorr cyclocondensation and nitration of benzene.