Description
4-Ethoxybenzophenone (CAS No. 27982-06-5) is a high-purity organic compound with the molecular formula C15H14O2. This aromatic ketone features a benzophenone core substituted with an ethoxy group at the para position, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its crystalline solid form and well-characterized properties ensure consistency for laboratory and industrial applications. Ideal for UV-absorbing formulations, photoinitiators, and as a building block for specialty chemicals, this compound is rigorously tested for purity and stability. Packaged under inert conditions to prevent degradation, it is suitable for researchers requiring reliable and reproducible results.
Properties
- CAS Number: 27982-06-5
- Complexity: 235
- IUPAC Name: (4-ethoxyphenyl)-phenyl-methanone
- InChI: InChI=1S/C15H14O2/c1-2-17-14-10-8-13(9-11-14)15(16)12-6-4-3-5-7-12/h3-11H,2H2,1H3
- InChI Key: IBRIFDGHXDFGBY-UHFFFAOYSA-N
- Exact Mass: 226.099379685
- Molecular Formula: C15H14O2
- Molecular Weight: 226.27
- SMILES: CCOC1=CC=C(C=C1)C(=O)C2=CC=CC=C2
- Topological: 26.3
- Monoisotopic Mass: 226.099379685
- Synonyms: 4-Ethoxybenzophenone, 27982-06-5, (4-ethoxyphenyl)(phenyl)methanone, (4-ETHOXYPHENYL)PHENYLMETHANONE, (4-ethoxyphenyl)-phenylmethanone, Methanone, (4-ethoxyphenyl)phenyl-, NSC64687, 4-Aethoxybenzophenon, MFCD00568422, NCIOpen2_002935, SCHEMBL845256, SCHEMBL11361262, SCHEMBL16600542, SCHEMBL16600543, DTXSID40289817, CL8667, NSC-64687, AKOS008948192, AS-46068
4-Ethoxybenzophenone is widely used as a UV absorber in coatings, plastics, and personal care products due to its ability to absorb ultraviolet light effectively. In pharmaceutical research, it serves as a key intermediate in the synthesis of bioactive molecules and drug candidates. Additionally, it is employed in photoinitiator systems for polymerization reactions, enhancing efficiency in industrial processes. Its stability under various conditions makes it a preferred choice for high-performance applications in material science and chemical synthesis.
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