| Identification | Back 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 Properties | Back 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 Data | Back 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 Information | Back 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 |
|
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Energy Chemical
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TCI Europe
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TCI AMERICA
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