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Details

Stereochemistry RACEMIC
Molecular Formula C15H19NO
Molecular Weight 229.3175
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FURFENOREX, (±)-

SMILES

CC(CC1=CC=CC=C1)N(C)CC2=CC=CO2

InChI

InChIKey=DLGIIZAHQPTVCJ-UHFFFAOYSA-N
InChI=1S/C15H19NO/c1-13(11-14-7-4-3-5-8-14)16(2)12-15-9-6-10-17-15/h3-10,13H,11-12H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C15H19NO
Molecular Weight 229.3175
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 08:35:21 GMT 2023
Edited
by admin
on Sat Dec 16 08:35:21 GMT 2023
Record UNII
554JE75W4N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FURFENOREX, (±)-
Common Name English
DL-FURFENOREX
Common Name English
2-FURANMETHANAMINE, N-METHYL-N-(1-METHYL-2-PHENYLETHYL)-
Systematic Name English
FURFURYLMETHYLAMPHETAMINE DL-FORM
MI  
Common Name English
FURFURYLMETHYLAMPHETAMINE
Systematic Name English
FURFURYLMETHYLAMPHETAMINE DL-FORM [MI]
Common Name English
Code System Code Type Description
MERCK INDEX
m195
Created by admin on Sat Dec 16 08:35:22 GMT 2023 , Edited by admin on Sat Dec 16 08:35:22 GMT 2023
PRIMARY Merck Index
FDA UNII
554JE75W4N
Created by admin on Sat Dec 16 08:35:22 GMT 2023 , Edited by admin on Sat Dec 16 08:35:22 GMT 2023
PRIMARY
CAS
14817-79-9
Created by admin on Sat Dec 16 08:35:22 GMT 2023 , Edited by admin on Sat Dec 16 08:35:22 GMT 2023
SUPERSEDED
PUBCHEM
26762
Created by admin on Sat Dec 16 08:35:22 GMT 2023 , Edited by admin on Sat Dec 16 08:35:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID3057727
Created by admin on Sat Dec 16 08:35:22 GMT 2023 , Edited by admin on Sat Dec 16 08:35:22 GMT 2023
PRIMARY
CAS
13445-60-8
Created by admin on Sat Dec 16 08:35:22 GMT 2023 , Edited by admin on Sat Dec 16 08:35:22 GMT 2023
PRIMARY
WIKIPEDIA
Furfenorex
Created by admin on Sat Dec 16 08:35:22 GMT 2023 , Edited by admin on Sat Dec 16 08:35:22 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY