Propiophenone

Propiophenone

Names
Preferred IUPAC name 1-Phenylpropan-1-one
Other names Ethyl phenyl ketone, BzEt
Identifiers
CAS Number	93-55-0 Y
3D model ( JSmol )	Interactive image
ChEBI	CHEBI:425902 Y
ChEMBL	ChEMBL193446 Y
ChemSpider	6881 Y
ECHA InfoCard	100.002.053
PubChem CID	7148
UNII	E599A8OKQH Y
CompTox Dashboard (EPA)	DTXSID2044470
InChI InChI=1S/C9H10O/c1-2-9(10)8-6-4-3-5-7-8/h3-7H,2H2,1H3 Y Key: KRIOVPPHQSLHCZ-UHFFFAOYSA-N Y InChI=1/C9H10O/c1-2-9(10)8-6-4-3-5-7-8/h3-7H,2H2,1H3 Key: KRIOVPPHQSLHCZ-UHFFFAOYAT
SMILES CCC(=O)c1ccccc1
Properties
Chemical formula	C9H10O
Molar mass	134.178 g·mol−1
Appearance	Colorless liquid
Density	1.0087 g/mL
Melting point	18.6 °C (65.5 °F; 291.8 K)
Boiling point	218 °C (424 °F; 491 K)
Solubility in water	Insoluble
Magnetic susceptibility (χ)	-83.73·10−6 cm3/mol
Related compounds
Related ketones	Acetophenone Butyrophenone
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is YN ?) Infobox references

Propiophenone (

Production

Propiophenone can be prepared by

It is an intermediate in the synthesis of the pharmaceuticals phenmetrazine and propoxyphen.^[1][4][5]

Other drugs made from propiophenone include the following: PDM-35, Eprazinone, Methcathinone (leading to ephedrine), Trimebutine, Amfepramone, Diphepanol, Metamfepramone, Etoxadrol, Hydroxyphenamate, Phendimetrazine, Iminophenimide, Bencisteine, Flumecinol, Pyrroliphene, Perisone,

References