2-(5-METHOXY-1-BENZOFURAN-3-YL)-N,N-DIMETHYLETHANAMINE

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	MOL RATIO 1 MOL RATIO (average)

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

Substance Class	Chemical
Record UNII	9JXZ3RM7Y9
Record Status	`Validated (UNII)`
Record Version

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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

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Classification Tree

Code System

Code

Psychedelics

WIKIPEDIA

Designer-drugs-Dimemebfe

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Code System

Code

Type

Description

FDA UNII

9JXZ3RM7Y9

PRIMARY

EPA CompTox

DTXSID80161481

PRIMARY

WIKIPEDIA

Dimemebfe

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

PRIMARY

PUBCHEM

126589

PRIMARY

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