Description

(Z)-Prop-1-en-1-ylboronic acid (CAS: 7547-96-8) is a high-purity boronic acid derivative with the molecular formula C₃H₇BO₂. This organoboron compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its stability and reactivity. The (Z)-configuration ensures selective transformations, making it a valuable reagent for constructing complex molecular architectures. Suitable for research and industrial applications, this product is rigorously tested to meet ≥95.0% purity standards. It is available in various quantities to accommodate both small-scale laboratory use and bulk manufacturing processes.

Properties

• CAS Number: 7547-96-8
• Complexity: 50.8
• IUPAC Name: [(Z)-prop-1-enyl]boronic acid
• InChI: InChI=1S/C3H7BO2/c1-2-3-4(5)6/h2-3,5-6H,1H3/b3-2-
• InChI Key: CBMCZKMIOZYAHS-IHWYPQMZSA-N
• Exact Mass: 86.0539096
• Molecular Formula: C3H7BO2
• Molecular Weight: 85.90
• SMILES: B(/C=CC)(O)O
• Topological: 40.5
• Monoisotopic Mass: 86.0539096
• Synonyms: 7547-96-8, cis-Propenylboronic acid, cis-1-Propene-1-boronic acid, (Z)-Prop-1-en-1-ylboronic acid, cis-1-Propen-1-ylboronic acid, [(Z)-prop-1-enyl]boronic acid, 6336-44-3, (Z)-1-propenylboronic acid, NSC39118, MFCD04039917, cis-propene boronic acid, cis-propenyl boronic acid, (Z)-propenylboronic acid, cis-1-propenylboronic acid, SCHEMBL98277, (Z)-prop-1-enylboronic acid, (Z)-prop-1-enyl boronic acid, CBMCZKMIOZYAHS-IHWYPQMZSA-N, (1Z)-1-propen-1-ylboronic acid, CIS-1-PROPENE-1-BORONICACID, NSC-39118, (1Z)-prop-1-en-1-yl boronic acid, AKOS015836299, FP151149, cis-1-Propen-1-ylboronic acid, >=95.0%, CS-0129385, D78549

(Z)-Prop-1-en-1-ylboronic acid is primarily employed in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds, enabling the synthesis of pharmaceuticals and fine chemicals. Its cis-configuration allows for stereoselective transformations in organic chemistry. Researchers also use it in the development of boron-containing polymers and materials science applications. Suitable for catalytic and stoichiometric reactions, this compound is a versatile tool in synthetic chemistry.

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