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Details

Stereochemistry RACEMIC
Molecular Formula C14H19NO3
Molecular Weight 249.3056
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0
Stereo Comments Assumed racemic

SHOW SMILES / InChI
Structure of N-ETHYLPENTYLONE

SMILES

CCCC(NCC)C(=O)C1=CC2=C(OCO2)C=C1

InChI

InChIKey=VERDHJIMZYXGIW-UHFFFAOYSA-N
InChI=1S/C14H19NO3/c1-3-5-11(15-4-2)14(16)10-6-7-12-13(8-10)18-9-17-12/h6-8,11,15H,3-5,9H2,1-2H3

HIDE SMILES / InChI

Approval Year

Name Type Language
N-ETHYLPENTYLONE
Common Name English
.BETA.K-EBDP
Common Name English
1-PENTANONE, 1-(1,3-BENZODIOXOL-5-YL)-2-(ETHYLAMINO)-
Systematic Name English
EPHYLONE
Common Name English
.BETA.K-ETHYL-K
Common Name English
1-(1,3-BENZODIOXOL-5-YL)-2-(ETHYLAMINO)-PENTAN-1-ON
Common Name English
Classification Tree Code System Code
DEA NO. 7543
Created by admin on Sat Dec 16 10:24:20 GMT 2023 , Edited by admin on Sat Dec 16 10:24:20 GMT 2023
WIKIPEDIA Designer-drugs-Ephylone
Created by admin on Sat Dec 16 10:24:20 GMT 2023 , Edited by admin on Sat Dec 16 10:24:20 GMT 2023
Code System Code Type Description
PUBCHEM
57359308
Created by admin on Sat Dec 16 10:24:20 GMT 2023 , Edited by admin on Sat Dec 16 10:24:20 GMT 2023
PRIMARY
CAS
727641-67-0
Created by admin on Sat Dec 16 10:24:20 GMT 2023 , Edited by admin on Sat Dec 16 10:24:20 GMT 2023
PRIMARY
FDA UNII
D3H9D57JV9
Created by admin on Sat Dec 16 10:24:20 GMT 2023 , Edited by admin on Sat Dec 16 10:24:20 GMT 2023
PRIMARY
SMS_ID
100000174495
Created by admin on Sat Dec 16 10:24:20 GMT 2023 , Edited by admin on Sat Dec 16 10:24:20 GMT 2023
PRIMARY
WEB RESOURCE
N-ETHYLPENTYLONE
Created by admin on Sat Dec 16 10:24:20 GMT 2023 , Edited by admin on Sat Dec 16 10:24:20 GMT 2023
PRIMARY Thread: Novel stimulant Ephylone (N-Ethyl-Pentylone, βk-Ethyl-K, βk-EBDP)
EPA CompTox
DTXSID701336299
Created by admin on Sat Dec 16 10:24:20 GMT 2023 , Edited by admin on Sat Dec 16 10:24:20 GMT 2023
PRIMARY
WIKIPEDIA
N-Ethylpentylone
Created by admin on Sat Dec 16 10:24:20 GMT 2023 , Edited by admin on Sat Dec 16 10:24:20 GMT 2023
PRIMARY