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Details

Stereochemistry ACHIRAL
Molecular Formula C11H17NO3.ClH
Molecular Weight 247.719
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,4,5-TRIMETHOXYPHENETHYLAMINE HYDROCHLORIDE

SMILES

Cl.COC1=CC(CCN)=C(OC)C=C1OC

InChI

InChIKey=DFYVOIRUHMFAKR-UHFFFAOYSA-N
InChI=1S/C11H17NO3.ClH/c1-13-9-7-11(15-3)10(14-2)6-8(9)4-5-12;/h6-7H,4-5,12H2,1-3H3;1H

HIDE SMILES / InChI

Molecular Formula C11H17NO3
Molecular Weight 211.2576
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Patents

Patents

Substance Class Chemical
Created
by admin
on Tue Oct 22 13:36:16 UTC 2019
Edited
by admin
on Tue Oct 22 13:36:16 UTC 2019
Record UNII
03IY6V9XQG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,4,5-TRIMETHOXYPHENETHYLAMINE HYDROCHLORIDE
Systematic Name English
BENZENEETHANAMINE, 2,4,5-TRIMETHOXY-, HYDROCHLORIDE
Systematic Name English
PHENETHYLAMINE, 2,4,5-TRIMETHOXY-, HYDROCHLORIDE
Systematic Name English
2C-O HCL
Common Name English
BENZENEETHANAMINE, 2,4,5-TRIMETHOXY-, HYDROCHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
CAS
3166-78-7
Created by admin on Tue Oct 22 13:36:16 UTC 2019 , Edited by admin on Tue Oct 22 13:36:16 UTC 2019
PRIMARY
EPA CompTox
3166-78-7
Created by admin on Tue Oct 22 13:36:16 UTC 2019 , Edited by admin on Tue Oct 22 13:36:16 UTC 2019
PRIMARY
PUBCHEM
12515933
Created by admin on Tue Oct 22 13:36:16 UTC 2019 , Edited by admin on Tue Oct 22 13:36:16 UTC 2019
PRIMARY
Related Record Type Details
ACTIVE MOIETY
2C (2C-x) is a general name for the family of psychedelic phenethylamines containing methoxy groups on the 2 and 5 positions of a benzene ring. Most of these compounds also carry lipophilic substituents at the 4 position, usually resulting in more potent and more metabolically stable and longer acting compounds. Most of the currently known 2C compounds were first synthesized by Alexander Shulgin in the 1970s and 1980s, and published in his book, PiHKAL (Phenethylamines i Have Known And Loved). Dr. Shulgin also invented the term 2C, being an acronym for the 2 carbon atoms between the benzene ring and the amino group.[1] Shulgin, Alexander; Ann Shulgin (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.