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Details

Stereochemistry ACHIRAL
Molecular Formula C12H19NO2
Molecular Weight 209.2848
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2C-G

SMILES

COC1=CC(CCN)=C(OC)C(C)=C1C

InChI

InChIKey=NFOHGLKGLZIHJQ-UHFFFAOYSA-N
InChI=1S/C12H19NO2/c1-8-9(2)12(15-4)10(5-6-13)7-11(8)14-3/h7H,5-6,13H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C12H19NO2
Molecular Weight 209.2848
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Analytical characterization of three hallucinogenic N-(2-methoxy)benzyl derivatives of the 2C-series of phenethylamine drugs.
2013 Aug
Identification and characterization of 2,5-dimethoxy-3,4-dimethyl-β-phenethylamine (2C-G)--a new designer drug.
2013 Jul
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:36:18 UTC 2023
Edited
by admin
on Sat Dec 16 08:36:18 UTC 2023
Record UNII
DTG7FMO01J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2C-G
Common Name English
BENZENEETHANAMINE, 2,5-DIMETHOXY-3,4-DIMETHYL-
Systematic Name English
2,5-DIMETHOXY-3,4-DIMETHYLBENZENEETHANAMINE
Systematic Name English
2,5-DIMETHOXY-3,4-DIMETHYLPHENETHYLAMINE
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA PiHKAL
Created by admin on Sat Dec 16 08:36:18 UTC 2023 , Edited by admin on Sat Dec 16 08:36:18 UTC 2023
WIKIPEDIA Designer-drugs-2C-G
Created by admin on Sat Dec 16 08:36:18 UTC 2023 , Edited by admin on Sat Dec 16 08:36:18 UTC 2023
Code System Code Type Description
WIKIPEDIA
2C-G
Created by admin on Sat Dec 16 08:36:18 UTC 2023 , Edited by admin on Sat Dec 16 08:36:18 UTC 2023
PRIMARY 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.
EPA CompTox
DTXSID70174848
Created by admin on Sat Dec 16 08:36:18 UTC 2023 , Edited by admin on Sat Dec 16 08:36:18 UTC 2023
PRIMARY
CAS
207740-18-9
Created by admin on Sat Dec 16 08:36:18 UTC 2023 , Edited by admin on Sat Dec 16 08:36:18 UTC 2023
PRIMARY
FDA UNII
DTG7FMO01J
Created by admin on Sat Dec 16 08:36:18 UTC 2023 , Edited by admin on Sat Dec 16 08:36:18 UTC 2023
PRIMARY
PUBCHEM
22238091
Created by admin on Sat Dec 16 08:36:18 UTC 2023 , Edited by admin on Sat Dec 16 08:36:18 UTC 2023
PRIMARY
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