U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C10H13NO2
Molecular Weight 179.2157
Optical Activity ( + )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TENAMFETAMINE, (S)-

SMILES

C[C@H](N)CC1=CC=C2OCOC2=C1

InChI

InChIKey=NGBBVGZWCFBOGO-ZETCQYMHSA-N
InChI=1S/C10H13NO2/c1-7(11)4-8-2-3-9-10(5-8)13-6-12-9/h2-3,5,7H,4,6,11H2,1H3/t7-/m0/s1

HIDE SMILES / InChI

Molecular Formula C10H13NO2
Molecular Weight 179.2157
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 08:25:58 UTC 2023
Edited
by admin
on Sat Dec 16 08:25:58 UTC 2023
Record UNII
940U7323I4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TENAMFETAMINE, (S)-
Common Name English
1,3-BENZODIOXOLE-5-ETHANAMINE, .ALPHA.-METHYL-, (S)-
Systematic Name English
(S)-(+)-3,4-(METHYLENEDIOXY)AMPHETAMINE
Systematic Name English
D-3,4-METHYLENEDIOXYAMPHETAMINE
Systematic Name English
(S)-3,4-(METHYLENEDIOXY)AMPHETAMINE
Systematic Name English
MDA, (+)-
Common Name English
1,3-BENZODIOXOLE-5-ETHANAMINE, .ALPHA.-METHYL-, (.ALPHA.S)-
Systematic Name English
3,4-Methylenedioxyamphetamine, (S)-
Common Name English
TENAMFETAMINE, (+)-
Common Name English
MDA, (S)-
Common Name English
MDA (PSYCHEDELIC), (S)-
Common Name English
Code System Code Type Description
FDA UNII
940U7323I4
Created by admin on Sat Dec 16 08:25:58 UTC 2023 , Edited by admin on Sat Dec 16 08:25:58 UTC 2023
PRIMARY
EPA CompTox
DTXSID80215872
Created by admin on Sat Dec 16 08:25:58 UTC 2023 , Edited by admin on Sat Dec 16 08:25:58 UTC 2023
PRIMARY
CAS
65620-66-8
Created by admin on Sat Dec 16 08:25:58 UTC 2023 , Edited by admin on Sat Dec 16 08:25:58 UTC 2023
PRIMARY
PUBCHEM
3050061
Created by admin on Sat Dec 16 08:25:58 UTC 2023 , Edited by admin on Sat Dec 16 08:25:58 UTC 2023
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
SALT/SOLVATE -> PARENT
ENANTIOMER -> ENANTIOMER