Ethcathinone
| Ethcathinone | |
|---|---|
| |
| Molecular structure via molpic | |
| Molecular formula | C11H15NO |
| Molecular mass | 177.24 g/mol |
| Chirality | racemic |
| Identifiers [] | |
|---|---|
| IUPAC name | 2-(ethylamino)-1-phenylpropan-1-one |
| Cannonical SMILES | CCNC(C)C(=O)C1=CC=CC=C1 |
| InChI | InChI=1S/C11H15NO/c1-3-12-9(2)11(13)10-7-5-4-6-8-10/h4-9,12H,3H2,1-2H3 |
| InChIKey | LYMHIBZGTAPASQ-UHFFFAOYSA-N |
Ethcathinone (also known as ethylpropion, N-Ethylaminopropiophenone, 1-Phenyl-2-(ethylamino)-1-propanone, Ethylaminopropiophenone HCl, UR 1424, 1-Propanone, 2-(ethylamino)-1-phenyl-, CHEMBL3298876, 2-ethylamino-1-phenylpropan-1-one, ETH-CAT or N-Ethylcathinone) is a stimulant substance of the methcathinone class.
Chemistry
Ethcathinone is typically prepared in the form of its amine salts hydrochloride.
Ethcathinone is a racemic mixture of two optical stereoisomers.