CAS 5409-60-9
:4,4-Diphenyl-2-butanone
Description:
4,4-Diphenyl-2-butanone, with the CAS number 5409-60-9, is an organic compound characterized by its ketone functional group and a unique structure featuring two phenyl groups attached to a butanone backbone. This compound typically appears as a white to pale yellow crystalline solid and is known for its relatively high melting point. It is soluble in organic solvents such as ethanol and acetone but has limited solubility in water due to its hydrophobic phenyl groups. 4,4-Diphenyl-2-butanone is often utilized in organic synthesis and as an intermediate in the production of various pharmaceuticals and fine chemicals. Its reactivity is influenced by the presence of the carbonyl group, making it susceptible to nucleophilic attack. Additionally, it may exhibit interesting optical properties, making it a subject of study in materials science and photochemistry. Safety precautions should be taken when handling this compound, as with many organic chemicals, due to potential health hazards associated with exposure.
Formula:C16H16O
InChI:InChI=1S/C16H16O/c1-13(17)12-16(14-8-4-2-5-9-14)15-10-6-3-7-11-15/h2-11,16H,12H2,1H3
InChI key:InChIKey=FPHXYKLKNOEKTQ-UHFFFAOYSA-N
SMILES:C(CC(C)=O)(C1=CC=CC=C1)C2=CC=CC=C2
Synonyms:- 1,1-Diphenyl-3-butanone
- 2-Butanone, 4,4-diphenyl-
- 4,4-Diphenylbutan-2-one
- NSC 12496
- 4,4-Diphenyl-2-butanone
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Found 4 products.
4,4-Diphenyl-2-butanone, 98%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C16H16OPurity:98%Color and Shape:Crystals or powder or crystalline powder or lumps, White to creamMolecular weight:224.304,4'-Diphenyl-2-butanone
CAS:<p>4,4'-Diphenyl-2-butanone is a biomolecular reagent that is dehydrated to form an activated cyclic sulfide. This compound can be used in the preparation of β-unsaturated ketones and aldehydes. It is also used in the synthesis of methyl cinnamate, which can be converted to cinnamaldehyde. The condensation process of 4,4'-diphenyl-2-butanone with chloride yields trifluoromethylthiolation products such as 2,3-dichloro-5-(trifluoromethyl)benzenesulfonyl chloride. The reaction product can be used to synthesize rhenium complexes. It has been proposed that this reagent may be applied in the synthesis of rhenium complexes by reacting with chloride and then adding a ligand such as aluminium or β-unsaturated ketones.</p>Formula:C16H16OPurity:Min. 95%Color and Shape:PowderMolecular weight:224.3 g/mol



