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1134643-88-1

1134643-88-1 Structure

1134643-88-1 Structure
IdentificationBack Directory
[Name]

PotassiuM (Mix)-2-buten-2-yltrifluoroborate
[CAS]

1134643-88-1
[Synonyms]

Potassium (Z)-2-Buten-2-yltrifluoroborate
Potassium (Z)-but-2-en-2-yltrifluoroborate
PotassiuM (Mix)-2-buten-2-yltrifluoroborate
Potassium (2Z)-2-buten-2-yltrifluoroborate >=95%
Potassium (2Z)-2-buten-2-yl(trifluoro)borate(1-)
potassium:[(Z)-but-2-en-2-yl]-trifluoroboranuide
Borate(1-), trifluoro[(1Z)-1-methyl-1-propen-1-yl]-, potassium (1:1), (T-4)-
[Molecular Formula]

C4H7BF3K
[MDL Number]

MFCD16621473
[MOL File]

1134643-88-1.mol
[Molecular Weight]

162.003
Chemical PropertiesBack Directory
[Melting point ]

147-152°C
[storage temp. ]

2-8°C
[form ]

solid
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C4H7BF3.K/c1-3-4(2)5(6,7)8;/h3H,1-2H3;/q-1;+1/b4-3+;
[InChIKey]

IFJZXYDBLMMRCO-BJILWQEISA-N
[SMILES]

[K+].[B-](/C(=C/C)/C)(F)(F)F
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26
[WGK Germany ]

3
[HS Code ]

2931900090
Hazard InformationBack Directory
[Uses]

Potassium (2Z)-2-buten-2-yltrifluoroborate can be used as a substrate:
  • In the asymmetric alkenylation of imines/aldimines using a rhodium based catalyst.
  • In the Rh(I)-catalyzed allylic amines synthesis by reacting with N-tert-butanesulfinyl aldimines.
  • In the ytterbium triflate catalyzed multicomponent synthesis of β-unsaturated α-amino esters.

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