Description

Oct-7-enylboronic acid (CAS: 1198772-66-5) is a high-purity organoboron compound with the molecular formula C₈H₁₇BO₂. This versatile boronic acid derivative features a terminal alkene group, making it an essential building block for Suzuki-Miyaura cross-coupling reactions, a cornerstone of modern synthetic organic chemistry. Our product is rigorously tested to ensure superior quality, with ≥95% purity by HPLC, and is supplied as a white to off-white crystalline solid. Ideal for pharmaceutical research, materials science, and catalysis studies, Oct-7-enylboronic acid is packaged under inert gas to ensure stability and longevity. Each batch is accompanied by comprehensive analytical data (NMR, MS, and FTIR) for quality assurance.

Properties

• CAS Number: 1198772-66-5
• Complexity: 94.1
• IUPAC Name: oct-7-enylboronic acid
• InChI: InChI=1S/C8H17BO2/c1-2-3-4-5-6-7-8-9(10)11/h2,10-11H,1,3-8H2
• InChI Key: NWZXPKHHIAAANV-UHFFFAOYSA-N
• Exact Mass: 156.1321599
• Molecular Formula: C8H17BO2
• Molecular Weight: 156.03
• SMILES: B(CCCCCCC=C)(O)O
• Topological: 40.5
• Monoisotopic Mass: 156.1321599
• Synonyms: OCT-7-ENYLBORONIC ACID, 1198772-66-5, OCT-7-EN-1-YLBORONIC ACID, Boronic acid, B-7-octen-1-yl-, MFCD16660277, Oct-7-en ylboronic acid, SCHEMBL3325574, DTXSID90681529, AKOS006333917, BS-20008, DB-266581, CS-0175084, G70444

Application

Oct-7-enylboronic acid is widely used in palladium-catalyzed cross-coupling reactions to form carbon-carbon bonds, particularly in the synthesis of complex organic molecules. Its terminal alkene functionality allows for further derivatization via hydroboration or metathesis reactions. Researchers employ this compound in the development of novel pharmaceuticals, agrochemicals, and functional materials. It also serves as a key intermediate in the preparation of boron-containing polymers and sensors.

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