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7547-96-8

(Z);-Prop-1-en-1-ylboronic acid

Catalog#: AR003DEQ  |   CAS#: 7547-96-8  |   MDL#: MFCD04039917  |   MF: C3H7BO2  |   MW: 85.8975

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Catalog Number AR003DEQ
Chemical Name (Z);-Prop-1-en-1-ylboronic acid
CAS Number 7547-96-8
Molecular Formula C3H7BO2
Molecular Weight 85.8975
MDL Number MFCD04039917
SMILES OB(/C=CC)O
NSC Number 39118

(Z)-Prop-1-en-1-ylboronic acid is a versatile organic compound commonly used in chemical synthesis as a valuable building block for creating complex molecules. Its unique structure and reactivity allow it to participate in a variety of important organic reactions, making it a powerful tool in the hands of synthetic chemists.One prominent application of (Z)-Prop-1-en-1-ylboronic acid is in cross-coupling reactions, particularly in Suzuki-Miyaura coupling. In this reaction, the boronic acid functionality of (Z)-Prop-1-en-1-ylboronic acid can form a boronate complex with a palladium catalyst, enabling the coupling with an organic halide or pseudohalide substrate to form a new carbon-carbon bond. This method is widely utilized in the synthesis of pharmaceuticals, agrochemicals, and materials science.Additionally, (Z)-Prop-1-en-1-ylboronic acid can undergo oxidative coupling reactions to produce biaryl compounds, which are important structural motifs found in many natural products and pharmaceuticals. Its ability to react selectively with various electrophiles also makes it a valuable reagent for functional group transformations and regioselective bond formation in organic synthesis.Overall, the application of (Z)-Prop-1-en-1-ylboronic acid in chemical synthesis offers synthetic chemists a versatile and efficient tool for constructing complex molecules with specific functionalities, further contributing to the advancement of diverse scientific fields.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class -
Packing Group -

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