Description

(9-(m-tolyl)-9H-carbazol-3-yl) boronic acid (CAS No. 1609267-35-7) is a high-purity boronic acid derivative featuring a carbazole core functionalized with a meta-tolyl group and a boronic acid moiety. With the molecular formula C₁₉H₁₆BNO₂, this compound is a valuable building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its IUPAC name, [9-(3-methylphenyl)carbazol-3-yl]boronic acid, reflects its precise structural configuration. This reagent is ideal for researchers developing advanced materials, pharmaceuticals, and optoelectronic compounds due to its stability and reactivity. Available in various quantities, it is rigorously tested for purity and consistency, ensuring reliable performance in sensitive applications.

Properties

• CAS Number: 1609267-35-7
• Complexity: 418
• IUPAC Name: [9-(m-tolyl)carbazol-3-yl]boronic acid
• InChI: InChI=1S/C19H16BNO2/c1-13-5-4-6-15(11-13)21-18-8-3-2-7-16(18)17-12-14(20(22)23)9-10-19(17)21/h2-12,22-23H,1H3
• InChI Key: TXMRJMSMDBSRHW-UHFFFAOYSA-N
• Exact Mass: 301.1274089
• Molecular Formula: C19H16BNO2
• Molecular Weight: 301.1
• SMILES: B(C1=CC2=C(C=C1)N(C3=CC=CC=C32)C4=CC=CC(=C4)C)(O)O
• Topological: 45.4
• Monoisotopic Mass: 301.1274089
• Synonyms: 1609267-35-7, (9-(m-tolyl)-9H -carbazol-3-yl) boronic acid, (9-(m-tolyl)-9H-carbazol-3-yl)boronic acid, DB-091300

Application

(9-(m-tolyl)-9H-carbazol-3-yl) boronic acid is widely used in palladium-catalyzed cross-coupling reactions to synthesize complex organic molecules, particularly in pharmaceutical and materials science research. Its carbazole backbone makes it suitable for constructing conjugated systems in organic electronics, such as OLEDs and photovoltaic materials. Researchers also employ it in the development of bioactive compounds due to its boronic acid group’s ability to form stable covalent bonds with diols and other functional groups.

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