| Identification | Back Directory | [Name]
Potassium (E)-propenyl-1-trifluoroborate | [CAS]
804565-39-7 | [Synonyms]
(e)-propenyl-1-trifluoroborate
trifluoro-[(E)-prop-1-enyl]boranuide
Potassium (E)-trifluoro(1-propenyl)borate
Potassium trifluoro(prop-1-en-1-yl)borate
Potassium trans-1-propenyltrifluoroborate
potassiuM (E)-trifluoro(prop-1-enyl)borate
PotassiuM (E)-1-propenyl-1-trifluoroborate
potassium trifluoro(prop-1-en-1-yl)boranuide
PotassiuM (E)-trifluoro(prop-1-en-1-yl)borate
potassium,trifluoro-[(E)-prop-1-enyl]boranuide | [Molecular Formula]
C3H5BF3K | [MDL Number]
MFCD09992882
| [MOL File]
804565-39-7.mol | [Molecular Weight]
147.976 |
| Chemical Properties | Back Directory | [Melting point ]
81-85°C | [form ]
solid | [InChI]
1S/C3H5BF3.K/c1-2-3-4(5,6)7;/h2-3H,1H3;/q-1;+1/b3-2+; | [InChIKey]
RLDWVFWDURMTAV-SQQVDAMQSA-N | [SMILES]
[K+].C\C=C\[B-](F)(F)F |
| Hazard Information | Back Directory | [Uses]
Potassium?trans-1-propenyltrifluoroborate can be used:
- As a substrate in the cross-coupling reactions with 2-(chloromethyl)-2,1-borazaronaphthalenes to yield allyl borazaronaphthalenes using a palladium catalyst.
- In the synthesis of anethole dithiolethione-NH2 (ADT-NH2), which in turn is used to prepare a drug-H2S delivery system.
- To prepare methyl (E)-2,2-dimethyl-5-(propen-1-yl)-4H-benzo[d][1,3]dioxine-7-carboxylate, a key intermediate for the synthesis of the alkaloid ampullosine.
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