2-Chloro-1,3-dimethylimidazolidinium tetrafluoroborate

Base Information

• Chemical Name: 2-Chloro-1,3-dimethylimidazolidinium tetrafluoroborate
• CAS No.: 153433-26-2
• Molecular Formula: C5H10BClF4N2
• Molecular Weight: 222.42
• Hs Code.: 29332900
• European Community (EC) Number: 623-751-1
• Mol file: 153433-26-2.mol

Synonyms:153433-26-2;2-Chloro-1,3-dimethylimidazolidinium tetrafluoroborate;2-Chloro-1,3-dimethyl-4,5-dihydroimidazolium tetrafluoroborate;cib reagent;2-Chloro-1,3-dimethylimidazolinium Tetrafluoroborate;C5H10BClF4N2;SCHEMBL5313803;MFCD09039291;AKOS025401721;AC-24867;AS-17501;C3444;2-Chloro-1,3-dimethylimidazolium tetrafluoroborate;A809424;J-508594;2-chloro-1,3-dimethyl-imidazolidin-1-ium;tetrafluoroborate;2-Chloro-1,3-dimethyl-4,5-dihydroimidazoliumtetrafluoroborate;2-chloro-1,3-dimethyl-4,5-dihydroimidazol-1-ium;2-Chloro-1,3-dimethyl-4,5-dihydro-1H-imidazol-3-ium tetrafluoroborate

Chemical Property of 2-Chloro-1,3-dimethylimidazolidinium tetrafluoroborate

Chemical Property:

• Melting Point: 175-177 °C(lit.)
• PSA: 6.25000
• LogP: 1.36560
• Storage Temp.: 2-8°C
• Sensitive.: Moisture & Light Sensitive
• Solubility.: acetonitrile: 0.1 g/mL, clear
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 0
• Exact Mass: 220.0561688
• Heavy Atom Count: 13
• Complexity: 135

Purity/Quality:

98% ^*data from raw suppliers

2-Chloro-1,3-dimethylimidazolidinium tetrafluoroborate ^*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: [B-](F)(F)(F)F.CN1CC[N+](=C1Cl)C
• Uses: 2-Chloro-1,3-dimethylimidazolium tetrafluoroborate is a reagent for esterification of C-terminal amino acids to Wang resin without racemization and for coupling α,α-dimethyl amino acids; and for preparation of the benzotriazol-1-yloxy derivative, a new coupling reagent. It is used as a reagent for esterification and peptide coupling of sterically hindered amino acids; preparation of efficient diazo-transfer reagents; oxidative insertion for palladium and nickel catalyst synthesis; and preparation of catalysts for use in coupling reactions. Reagent for: Esterification and peptide coupling of sterically hindered amino acids Preparation of efficient diazo-transfer reagents Oxidative insertion for palladium and nickel catalyst synthesis Preparation of catalysts for use in coupling reactions