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ChemicalBook--->CAS DataBase List--->153433-26-2

153433-26-2

153433-26-2 Structure

153433-26-2 Structure
IdentificationMore
[Name]

2-Chloro-1,3-dimethylimidazolidinium tetrafluoroborate
[CAS]

153433-26-2
[Synonyms]

2-CHLORO-1,3-DIMETHYL-2-IMIDAZOLINIUM TETRAFLUOROBORATE
2-CHLORO-1,3-DIMETHYLIMIDAZOLIDINIUM BF4
2-CHLORO-1,3-DIMETHYLIMIDAZOLIDINIUM TETRAFLUOROBORATE
CIB
CIB REAGENT
2-CHLORO-1 3-DIMETHYL-2-IMIDAZOLINIUM &
2-Chloro-1,3-dimethylimidazolidiniumtetrafluorobo
CIB2-Chloro-1,3-dimethylimidazolidiniumtetrafluoroborate
CHRYSOPHANOL
[EINECS(EC#)]

623-751-1
[Molecular Formula]

C5H12BClF4N2
[MDL Number]

MFCD00210033
[Molecular Weight]

222.42
[MOL File]

153433-26-2.mol
Chemical PropertiesBack Directory
[Melting point ]

175-177 °C(lit.)
[storage temp. ]

2-8°C
[solubility ]

acetonitrile: 0.1 g/mL, clear
[form ]

Powder or Crystalline Powder
[color ]

White to off-white
[Sensitive ]

Moisture & Light Sensitive
[InChIKey]

UPLXKEIRISBKRM-UHFFFAOYSA-N
[CAS DataBase Reference]

153433-26-2(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[F ]

8-10-21
[HS Code ]

29332900
Hazard InformationBack Directory
[Chemical Properties]

Colorless to white crystalline powder
[Uses]

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
[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.
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

153433-26-2(sigmaaldrich)
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