Description
6,9-Diphenyl-9H-carbazole-3-boronic Acid (contains varying amounts of Anhydride) is a high-purity boronic acid derivative designed for advanced research and industrial applications. With the molecular formula C24H18BNO2, this compound serves as a critical intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for constructing complex carbazole-based frameworks. Its unique diphenylcarbazole structure enhances electronic properties, making it valuable in materials science, OLED development, and pharmaceutical research. The product is rigorously tested for quality, ensuring optimal performance in sensitive applications. Supplied as a fine powder with varying anhydride content, it is stored under inert conditions to maintain stability and reactivity.
Properties
- CAS Number: 1133058-06-6
- Complexity: 517
- IUPAC Name: (6,9-diphenylcarbazol-3-yl)boronic acid
- InChI: InChI=1S/C24H18BNO2/c27-25(28)19-12-14-24-22(16-19)21-15-18(17-7-3-1-4-8-17)11-13-23(21)26(24)20-9-5-2-6-10-20/h1-16,27-28H
- InChI Key: AIDQRXUWQFRMAQ-UHFFFAOYSA-N
- Exact Mass: 363.1430590
- Molecular Formula: C24H18BNO2
- Molecular Weight: 363.2
- SMILES: B(C1=CC2=C(C=C1)N(C3=C2C=C(C=C3)C4=CC=CC=C4)C5=CC=CC=C5)(O)O
- Topological: 45.4
- Monoisotopic Mass: 363.1430590
- Synonyms: 6,9-Diphenyl-9H-carbazole-3-boronic Acid (contains varying amounts of Anhydride), 835-259-6, 1133058-06-6, 6,9-Diphenyl-9H-carbazol-3-yl-3-boronic acid, (6,9-Diphenyl-9H-carbazol-3-yl)boronic acid, B-(6,9-Diphenyl-9H-carbazol-3-yl)boronic acid, (6,9-diphenylcarbazol-3-yl)boronic acid, 6,9-Diphenyl-9H-carbazol-3-yl-3-boronic acid;B-(6,9-diphenyl-9H-carbazol-3-yl)-boronic acid, MFCD22123650, SCHEMBL322024, DTXSID80732751, AIDQRXUWQFRMAQ-UHFFFAOYSA-N, CS-B1256, AKOS016003421, AS-55564, 6,9-diphenyl-9H-carbazole-3-boronic acid, D4779, 6,9-Diphenyl-9H-carbazol-3-yl-3-boronicacid, B-(6,9-Diphenyl-9H-carbazol-3-yl)-boronicacid, 6 pound not9-Diphenyl-9H-carbazol-3-yl-3-boronic acid
This compound is widely used in organic synthesis, particularly as a key building block for Suzuki-Miyaura cross-coupling reactions to create carbazole-based polymers and small molecules. Its applications extend to the development of organic semiconductors, OLED emitters, and photoelectric materials due to its electron-rich structure. Researchers also utilize it in medicinal chemistry for designing novel pharmacophores with enhanced binding properties.
Safety and Hazards
GHS Hazard Statements
- H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
- H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
Precautionary Statements
- P264, P264+P265, P280, P302+P352, P305+P351+P338, P321, P332+P317, P337+P317, and P362+P364
Hazard Classes and Categories
- Skin Irrit. 2 (100%)
- Eye Irrit. 2 (100%)
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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


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