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Quality Product Phenylethane Boronic Acid丨CAS 34420-17-2
Phenylethane Boronic Acid, CAS 34420-17-2, is an organoboron compound used as a specialized building block in organic synthesis. Its boronic acid functionality provides a versatile reaction site for carbon–carbon bond formation and the preparation of more complex organoboron derivatives. Depending on the specific synthetic route, it can support the development of substituted organic molecules and functional intermediates. Organoboron compounds are widely used in modern synthetic chemistry because of their compatibility with established transformations, particularly palladium-catalyzed cross-coupling reactions. Phenylethane Boronic Acid is therefore relevant to pharmaceutical research, specialty chemical development, and advanced organic synthesis.
Chemical Identifiers
| InChI | 1S/C8H11BO2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-5,10-11H,6-7H2 |
| InChI Key | VPRUMANMDWQMNF-UHFFFAOYSA-N |
| Smiles | OB(CCC1=CC=CC=C1)O |
| EC No. | 672-926-9 |
| MDL No. | MFCD01631226 |
| PubChem CID | 65389 |
Applications
Applications in Pharmaceutical Intermediate Synthesis
Organoboron building blocks play an important role in medicinal chemistry, where controlled carbon–carbon bond formation is essential for constructing complex molecular frameworks. Phenylethane Boronic Acid can be considered for synthetic routes involving boron-mediated transformations and the preparation of functionalized intermediates. Such chemistry supports the exploration of new molecular structures and the modification of existing scaffolds. Its potential application in pharmaceutical research depends on the target structure, reaction compatibility, and the requirements of the overall synthetic route.
Applications in Organic Synthesis
Boronic acid functionality is widely utilized in organic synthesis because it can participate in transformations with suitable organic electrophiles. Under appropriate conditions, organoboron compounds can be employed in palladium-catalyzed Suzuki–Miyaura coupling and related carbon–carbon bond-forming reactions. Phenylethane Boronic Acid may serve as a building block for developing substituted organic compounds and extending molecular frameworks. Its use can help researchers explore different synthetic pathways and prepare intermediates for subsequent functional-group transformations.
Applications in Specialty Chemical Development
The preparation of specialty chemicals often requires building blocks that offer selective reactivity and flexibility during multi-step synthesis. Phenylethane Boronic Acid can contribute to the development of customized organic intermediates through suitable organoboron chemistry. It may be incorporated into synthetic strategies designed to construct more elaborate molecular structures for industrial research and specialty chemical applications. Its value lies in providing an additional route for molecular modification and structural diversification.
Applications in Materials and Functional Molecule Research
Organoboron compounds are important tools in the preparation of functional organic molecules and advanced material intermediates. Their use in carbon–carbon coupling reactions enables researchers to assemble larger molecular structures from simpler building blocks. Phenylethane Boronic Acid may be explored in synthetic studies involving functional aromatic compounds, molecular frameworks, and customized material precursors. The suitability of the compound for a particular material application depends on the target structure and the chemistry used to incorporate its boron-containing functionality.
