Potassium 3-(N,N-diethylamino)prop-1-en-2-yltrifluoroborate is an organoboron compound characterized by the presence of a trifluoroborate group and a diethylamino substituent on a propene backbone. This compound typically appears as a solid or crystalline material and is soluble in polar organic solvents. The trifluoroborate moiety imparts unique reactivity, making it useful in various synthetic applications, particularly in organic synthesis and as a reagent in cross-coupling reactions. The presence of the diethylamino group enhances its nucleophilicity, allowing it to participate in reactions with electrophiles. Additionally, the compound is likely to exhibit stability under standard laboratory conditions, although it may be sensitive to moisture and air due to the reactive nature of the boron center. Its applications may extend to medicinal chemistry and materials science, where organoboron compounds are increasingly utilized for their versatile reactivity and functionalization potential. Safety precautions should be observed when handling this compound, as with all organoboron reagents, due to potential toxicity and reactivity.

PotassiuM 3-(N,N-diethylaMino)prop-1-en-2-yltrifluoroborate

1357559-54-6: Potassium 3-(N,N-diethylamino)prop-1-en-2-yltrifluoroborate is an organoboron compound characterized by the presence of a trifluoroborate group and a diethylamino substituent on a propene backbone. This compound typically appears as a solid or crystalline material and is soluble in polar organic solvents. The trifluoroborate moiety imparts unique reactivity, making it useful in various synthetic applications, particularly in organic synthesis and as a reagent in cross-coupling reactions. The presence of the diethylamino group enhances its nucleophilicity, allowing it to participate in reactions with electrophiles. Additionally, the compound is likely to exhibit stability under standard laboratory conditions, although it may be sensitive to moisture and air due to the reactive nature of the boron center. Its applications may extend to medicinal chemistry and materials science, where organoboron compounds are increasingly utilized for their versatile reactivity and functionalization potential. Safety precautions should be observed when handling this compound, as with all organoboron reagents, due to potential toxicity and reactivity.

CAS 1357559-54-6

PotassiuM 3-(N,N-diethylaMino)prop-1-en-2-yltrifluoroborate