CAS 4495-66-3
:1-[4-(Phenylmethoxy)phenyl]-1-propanone
Description:
1-[4-(Phenylmethoxy)phenyl]-1-propanone, also known by its CAS number 4495-66-3, is an organic compound characterized by its ketone functional group and a complex aromatic structure. This compound features a propanone backbone with a phenylmethoxy group attached to one of the aromatic rings, contributing to its unique chemical properties. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents such as ethanol and acetone, while being less soluble in water due to its hydrophobic aromatic components. The presence of multiple aromatic rings suggests potential for π-π stacking interactions, which can influence its reactivity and stability. This compound may be utilized in various applications, including organic synthesis and as an intermediate in the production of pharmaceuticals or other fine chemicals. As with many organic compounds, handling should be done with care, considering potential health hazards and the need for appropriate safety measures.
Formula:C16H16O2
InChI:InChI=1S/C16H16O2/c1-2-16(17)14-8-10-15(11-9-14)18-12-13-6-4-3-5-7-13/h3-11H,2,12H2,1H3
InChI key:InChIKey=IKFGSOJYHVTNDV-UHFFFAOYSA-N
SMILES:C(CC)(=O)C1=CC=C(OCC2=CC=CC=C2)C=C1
Synonyms:- 1-(4-Benzyloxyphenyl)propan-1-one
- 1-Propanone, 1-[4-(phenylmethoxy)phenyl]-
- 1-[4-(Benzyloxy)Phenyl]Propan-1-One
- 1-[4-(Phenylmethoxy)phenyl]-1-propanone
- 4′-(Benzyloxy)propiophenone
- NSC 41188
- Propiophenone, 4′-(benzyloxy)-
- p-Benzyloxypropiophenone
- 4-Benzyloxypropiophenone
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Found 5 products.
4-Benzyloxypropiophenone
CAS:Formula:C16H16O2Purity:97%Color and Shape:SolidMolecular weight:240.29704-Benzyloxypropiophenone
CAS:Formula:C16H16O2Purity:98.0%Color and Shape:Liquid, No data available.Molecular weight:240.3021-[4-(Benzyloxy)phenyl]propan-1-one
CAS:1-[4-(Benzyloxy)phenyl]propan-1-onePurity:98%Color and Shape:SolidMolecular weight:240.30g/mol4-Benzyloxypropiophenone
CAS:<p>4-Benzyloxypropiophenone is a receptor binding compound that has been shown to be a potent estrogen receptor modulator. It is an analog of propiophenone, a natural product derived from the seeds of the plant Acacia rigidula. 4-Benzyloxypropiophenone binds to the estrogen receptor and competes with estradiol for binding sites. This inhibits the growth of cancer cells by altering their proliferative response to estrogen. 4-Benzyloxypropiophenone also has cardiac effects and can inhibit the synthesis of cholesterol in human liver cells.</p>Formula:C16H16O2Purity:Min. 95%Color and Shape:PowderMolecular weight:240.3 g/mol




