CAS 466-37-5
:1,2,2,2-Tetraphenylethanone
Description:
1,2,2,2-Tetraphenylethanone, with the CAS number 466-37-5, is an organic compound characterized by its structure, which features a central carbon atom bonded to two phenyl groups and a carbonyl group (ketone). This compound is typically a white to pale yellow crystalline solid at room temperature. It is known for its stability and relatively low reactivity under standard conditions, making it useful in various applications, including organic synthesis and as a reagent in chemical reactions. The presence of multiple phenyl groups contributes to its unique physical properties, such as a high melting point and significant solubility in organic solvents. Additionally, 1,2,2,2-tetraphenylethanone exhibits interesting photophysical properties, which can be exploited in materials science and photochemistry. Its synthesis often involves the Friedel-Crafts acylation reaction, highlighting its relevance in synthetic organic chemistry. Safety precautions should be observed when handling this compound, as with many organic chemicals, due to potential health hazards associated with exposure.
Formula:C26H20O
InChI:InChI=1S/C26H20O/c27-25(21-13-5-1-6-14-21)26(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24/h1-20H
InChI key:InChIKey=CFBBKHROQRFCNZ-UHFFFAOYSA-N
SMILES:C(C(=O)C1=CC=CC=C1)(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4
Synonyms:- β-Benzopinacolone
- Acetophenone, 2,2,2-triphenyl-
- Ethanone, tetraphenyl-
- Ethanone, 1,2,2,2-tetraphenyl-
- 1,2,2,2-Tetraphenylethanone
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Found 6 products.
2,2,2-Triphenylacetophenone
CAS:Formula:C26H20OPurity:>99.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:348.452,2,2-Triphenylacetophenone
CAS:Formula:C26H20OPurity:99%Color and Shape:SolidMolecular weight:348.43642,2,2-Triphenylacetophenone
CAS:<p>2,2,2-Triphenylacetophenone</p>Purity:99%Molecular weight:348.45g/mol2,2,2-Triphenylacetophenone
CAS:Controlled Product<p>Applications 2,2,2-Triphenylacetophenone is an endocrine disrupter that is medicated through estrogen receptors.<br>References Roncaglioni, A., et al.: SAR. QSAR. Environ. Res., 19, 697 (2008); Kuzmanich, G., et al.: Photochem. Photobiol., 10, 1731 (2011);<br></p>Formula:C26H20OColor and Shape:NeatMolecular weight:348.452,2,2-Triphenylacetophenone
CAS:<p>2,2,2-Triphenylacetophenone (TPAP) is an insoluble organic compound that is soluble in organic solvents. It can be prepared from phenol by the reaction of acetophenone with benzoyl chloride. TPAP has a high dielectric constant and is used as a solvent for polymers. This compound is also used as a hydrogen bond acceptor in the functional theory of acids and bases. The chemical structure of TPAP contains two electron-donating nitrogens that form a hydrogen bond with the anions found in polar solvents such as water or alcohols. These bonds are often responsible for the solubility of TPAP in these solvents. In addition, TPAP's functional groups allow it to participate in many organic reactions, including nucleophilic substitution reactions and oxidation reactions that produce chlorine atoms as byproducts.</p>Formula:C26H20OPurity:Min. 95%Molecular weight:348.44 g/mol





