Trans-3-Phenyl-1-propen-1-ylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a propenyl chain with a phenyl substituent. This compound typically exhibits a double bond configuration that is trans, indicating that the phenyl group and the boronic acid are on opposite sides of the double bond. It is known for its utility in organic synthesis, particularly in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a key method for forming carbon-carbon bonds. The boronic acid moiety allows for the formation of stable complexes with diols and is also involved in various biological applications due to its ability to interact with biomolecules. The compound is generally soluble in organic solvents and may exhibit moderate stability under standard laboratory conditions. Its reactivity and functional properties make it a valuable intermediate in the synthesis of pharmaceuticals and other complex organic molecules. Safety precautions should be taken when handling this compound, as with many organoboron compounds, due to potential reactivity and toxicity.

TRANS-3-PHENYL-1-PROPEN-1-YLBORONIC ACID

129423-29-6: Trans-3-Phenyl-1-propen-1-ylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a propenyl chain with a phenyl substituent. This compound typically exhibits a double bond configuration that is trans, indicating that the phenyl group and the boronic acid are on opposite sides of the double bond. It is known for its utility in organic synthesis, particularly in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a key method for forming carbon-carbon bonds. The boronic acid moiety allows for the formation of stable complexes with diols and is also involved in various biological applications due to its ability to interact with biomolecules. The compound is generally soluble in organic solvents and may exhibit moderate stability under standard laboratory conditions. Its reactivity and functional properties make it a valuable intermediate in the synthesis of pharmaceuticals and other complex organic molecules. Safety precautions should be taken when handling this compound, as with many organoboron compounds, due to potential reactivity and toxicity.

CAS 129423-29-6

TRANS-3-PHENYL-1-PROPEN-1-YLBORONIC ACID

Trans-3-phenylpropen-1-yl-boronic acid

Ref: IN-DA007NKP

trans-3-Phenyl-1-propen-1-ylboronic acid

Ref: 54-OR360214

TRANS-3-PHENYL-1-PROPEN-1-YLBORONIC ACID

Ref: 10-F853900