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263163-17-3

263163-17-3 Structure

263163-17-3 Structure
IdentificationBack Directory
[Name]

1 3-DI-TERT-BUTYLIMIDAZOLIUM TETRAFLUORO
[CAS]

263163-17-3
[Synonyms]

ItBu.HBF4
1,3-Bis(t-butyL
1 3-DI-TERT-BUTYLIMIDAZOLIUM TETRAFLUORO
1,3-DI-TERT-BUTYLIMIDAZOLIUM TETRAFLUOR&
1,3-Bis(t-butyl)imidazolium tetrafluoroborate
1,3-Bis(tert-butyl)imidazolium tetrafluoroborate
1,3-ditert-butylimidazol-1-ium:tetrafluoroborate
1,3-Di-t-butylimidazolium tetrafluoroborate, 97%
1,3-Di-tert-butylimidazolium Tetrafluoroborate >
1,3-Di-tert-butyliMidazoliuM tetrafluoroborate 97%
1,3-Di-tert-butyl-1H-imidazol-3-ium tetrafluoroborate
1,3-Di-tert-butylimidazolium Tetrafluoroborate
1,3-Bis(t-butyl)imidazolium tetrafluoroborate, min. 97% ItBuHBF4
1H-Imidazolium, 1,3-bis(1,1-dimethylethyl)-, tetrafluoroborate(1-) (1:1)
N,Nμ-Bis(tert-butyl)imidazolium tetrafluoroborate, 1,3-Bis(tert-butyl)-imidazol-2-ylidinium tetrafluoroborate
[Molecular Formula]

C11H21N2.BF4
[MDL Number]

MFCD07784425
[MOL File]

263163-17-3.mol
[Molecular Weight]

268.104
Chemical PropertiesBack Directory
[Melting point ]

157-198 °C
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

solid
[color ]

white to cream-colored
[Stability:]

hygroscopic
[InChI]

1S/C11H21N2.BF4/c1-10(2,3)12-7-8-13(9-12)11(4,5)6;2-1(3,4)5/h7-9H,1-6H3;/q+1;-1
[InChIKey]

OOFLHRYFPBGTPQ-UHFFFAOYSA-N
[SMILES]

F[B-](F)(F)F.CC(C)(C)n1cc[n+](c1)C(C)(C)C
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[RIDADR ]

1759
[WGK Germany ]

3
[HS Code ]

2933.29.9000
[HazardClass ]

8
[PackingGroup ]

III
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

1,3-Di-tert-butylimidazolium tetrafluoroborate may be used in the preparation of di-μ-iodobis(1,3-di-tert-butylimidazolin-2-ylidene)diiododipalladium(II), a palladium(II)-NHC complex, which can catalyze Mizoroki-Heck reaction.
[General Description]

1,3-Di-tert-butylimidazolium tetrafluoroborate is an N-heterocyclic carbene (NHC) compound that can be prepared by reacting paraformaldehyde with tert-butyl amine and hydrogen tetrafluoroborate (35% in water).
[reaction suitability]

reagent type: catalyst
Spectrum DetailBack Directory
[Spectrum Detail]

1 3-DI-TERT-BUTYLIMIDAZOLIUM TETRAFLUORO(263163-17-3)1HNMR
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