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Details

Stereochemistry ACHIRAL
Molecular Formula C13H17NO2
Molecular Weight 219.2796
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-(5-METHOXY-1-BENZOFURAN-3-YL)-N,N-DIMETHYLETHANAMINE

SMILES

COC1=CC2=C(OC=C2CCN(C)C)C=C1

InChI

InChIKey=WBPQJTBOQCCTFX-UHFFFAOYSA-N
InChI=1S/C13H17NO2/c1-14(2)7-6-10-9-16-13-5-4-11(15-3)8-12(10)13/h4-5,8-9H,6-7H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C13H17NO2
Molecular Weight 219.2796
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 10:15:29 UTC 2023
Edited
by admin
on Sat Dec 16 10:15:29 UTC 2023
Record UNII
9JXZ3RM7Y9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-(5-METHOXY-1-BENZOFURAN-3-YL)-N,N-DIMETHYLETHANAMINE
Systematic Name English
5-MEO-BFE
Common Name English
5-MEO-BENZOFURANETHANAMINE
Common Name English
DIMEMEBFE
Common Name English
3-BENZOFURANETHANAMINE, 5-METHOXY-N,N-DIMETHYL-
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-Dimemebfe
Created by admin on Sat Dec 16 10:15:29 UTC 2023 , Edited by admin on Sat Dec 16 10:15:29 UTC 2023
Code System Code Type Description
FDA UNII
9JXZ3RM7Y9
Created by admin on Sat Dec 16 10:15:29 UTC 2023 , Edited by admin on Sat Dec 16 10:15:29 UTC 2023
PRIMARY
EPA CompTox
DTXSID80161481
Created by admin on Sat Dec 16 10:15:29 UTC 2023 , Edited by admin on Sat Dec 16 10:15:29 UTC 2023
PRIMARY
WIKIPEDIA
Dimemebfe
Created by admin on Sat Dec 16 10:15:29 UTC 2023 , Edited by admin on Sat Dec 16 10:15:29 UTC 2023
PRIMARY Dimemebfe (5-MeO-BFE) is a recreational drug[1] and research chemical. It acts as an agonist for the 5-HT1A and 5-HT2 family of serotonin receptors. It is related in structure to the psychedelic tryptamine derivative 5-MeO-DMT, but with the indole nitrogen replaced by oxygen, making dimemebfe a benzofuran derivative. It is several times less potent as a serotonin agonist than 5-MeO-DMT and with relatively more activity at 5-HT1A, but still shows strongest effects at the 5-HT2 family of receptors.
CAS
140853-58-3
Created by admin on Sat Dec 16 10:15:29 UTC 2023 , Edited by admin on Sat Dec 16 10:15:29 UTC 2023
PRIMARY
PUBCHEM
126589
Created by admin on Sat Dec 16 10:15:29 UTC 2023 , Edited by admin on Sat Dec 16 10:15:29 UTC 2023
PRIMARY
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