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Details

Stereochemistry RACEMIC
Molecular Formula C12H19NO3
Molecular Weight 225.2842
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3,4,5-TRIMETHOXYAMPHETAMINE

SMILES

COC1=CC(CC(C)N)=CC(OC)=C1OC

InChI

InChIKey=WGTASENVNYJZBK-UHFFFAOYSA-N
InChI=1S/C12H19NO3/c1-8(13)5-9-6-10(14-2)12(16-4)11(7-9)15-3/h6-8H,5,13H2,1-4H3

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
3,4,5-TRIMETHOXYAMPHETAMINE
Systematic Name English
DL-3,4,5-TRIMETHOXYAMPHETAMINE
Common Name English
ALPHA-METHYLMESCALINE
Common Name English
(±)-1-(3,4,5-TRIMETHOXYPHENYL)-2-AMINOPROPANE
Systematic Name English
TMA (PSYCHEDELIC)
Common Name English
J13.144J
Code English
BENZENEETHANAMINE, 3,4,5-TRIMETHOXY-.ALPHA.-METHYL-
Systematic Name English
PHENETHYLAMINE, 3,4,5-TRIMETHOXY-.ALPHA.-METHYL-
Systematic Name English
.ALPHA.-METHYLMESCALINE
Common Name English
1-(3,4,5-TRIMETHOXYPHENYL)PROPAN-2-AMINE
Systematic Name English
1-METHYL-2-(3,4,5-TRIMETHOXYPHENYL)ETHYLAMINE
Systematic Name English
3,4,5-TRIMETHOXYAMPHETAMINE, DL-
Common Name English
Classification Tree Code System Code
DEA NO. 7390
Created by admin on Fri Dec 15 15:07:56 UTC 2023 , Edited by admin on Fri Dec 15 15:07:56 UTC 2023
WIKIPEDIA PiHKAL
Created by admin on Fri Dec 15 15:07:56 UTC 2023 , Edited by admin on Fri Dec 15 15:07:56 UTC 2023
Code System Code Type Description
CAS
1082-88-8
Created by admin on Fri Dec 15 15:07:56 UTC 2023 , Edited by admin on Fri Dec 15 15:07:56 UTC 2023
PRIMARY
PUBCHEM
31016
Created by admin on Fri Dec 15 15:07:56 UTC 2023 , Edited by admin on Fri Dec 15 15:07:56 UTC 2023
PRIMARY
WIKIPEDIA
Trimethoxyamphetamine
Created by admin on Fri Dec 15 15:07:56 UTC 2023 , Edited by admin on Fri Dec 15 15:07:56 UTC 2023
PRIMARY
EPA CompTox
DTXSID00862529
Created by admin on Fri Dec 15 15:07:56 UTC 2023 , Edited by admin on Fri Dec 15 15:07:56 UTC 2023
PRIMARY
FDA UNII
P2K02L3YON
Created by admin on Fri Dec 15 15:07:56 UTC 2023 , Edited by admin on Fri Dec 15 15:07:56 UTC 2023
PRIMARY
CAS
22199-17-3
Created by admin on Fri Dec 15 15:07:56 UTC 2023 , Edited by admin on Fri Dec 15 15:07:56 UTC 2023
SUPERSEDED
DRUG BANK
DB01516
Created by admin on Fri Dec 15 15:07:56 UTC 2023 , Edited by admin on Fri Dec 15 15:07:56 UTC 2023
PRIMARY
NIH
NCATS
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