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Substituted benzofurans: Difference between revisions

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Changed the formula in R2
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| 6-MBPB || H || H || H || H || CH<sub>2</sub>CH(NHCH<sub>3</sub>)CH<sub>2</sub>CH<sub>3</sub> || H || [[File:6-MBPB.svg|170px]]
| 6-MBPB || H || H || H || H || CH<sub>2</sub>CH(NHCH<sub>3</sub>)CH<sub>2</sub>CH<sub>3</sub> || H || [[File:6-MBPB.svg|170px]]
|-
|-
| F-2 || CH<sub>3</sub> || H<sub>2</sub> || H || OCH<sub>3</sub> || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || [[File:F-2.svg|170px]]
| F-2 || HCH<sub>3</sub> || H<sub>2</sub> || H || OCH<sub>3</sub> || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || [[File:F-2.svg|170px]]
|-
|-
| F-22 || (CH<sub>3</sub>)<sub>2</sub> || H<sub>2</sub> || H || OCH<sub>3</sub> || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || [[File:F-22.svg|170px]]
| F-22 || (CH<sub>3</sub>)<sub>2</sub> || H<sub>2</sub> || H || OCH<sub>3</sub> || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || [[File:F-22.svg|170px]]

Revision as of 19:57, 1 June 2020

This article is a stub.

As such, it may contain incomplete or wrong information. You can help by expanding it.

The benzofuran molecule
Generic structure of a benzofuran class molecule

Benzofurans are chemical compounds which contain a benzofuran ring in their structure. Most of the benzofurans are research chemicals, most commonly stimulants and entactogens, and are fairly new. Benzofuran compounds are often analogues of MDxx and tryptamine compounds where a benzofuran ring has replaced the benzodioxole ring structure or indole ring respectively.

List of benzofuran compounds

Compound R2 R3 R4 R5 R6 R7 Structure
2-APB CH2CH(NH2)CH3 H H H H H
2-MAPB CH2CH(NHCH3)CH3 H H H H H
2-EAPB CH2CH(NHCH2CH3)CH3 H H H H H
3-APB H CH2CH(NH2)CH3 H H H H
Mebfap H CH2CH(NH2)CH3 H OCH3 H H
5-MeO-BFE H CH2CH2N(CH3)2 H OCH3 H H
5-MeO-DiBF H CH2CH2N(CH(CH3)2)2 H OCH3 H H
4-APB H H CH2CH(NH2)CH3 H H H
DOB-5-hemifly H2 H2 CH2CH(NH2)CH3 OCH3 H Br
5-APB H H H CH2CH(NH2)CH3 H H
5-APDB H2 H2 H CH2CH(NH2)CH3 H H
5-MAPB H H H CH2CH(NHCH3)CH3 H H
5-MAPDB H2 H2 H CH2CH(NHCH3)CH3 H H
βk-5-MAPB H H H COCH(NHCH3)CH3 H H
5-EAPB H H H CH2CH(NHCH2CH3)CH3 H H
5-EAPDB H2 H2 H CH2CH(NHCH2CH3)CH3 H H
5-MBPB H H H CH2CH(NHCH3)CH2CH3 H H
5-DBFPV H2 H2 H COCH(NC4H8)CH2CH2CH3 H H
6-MeO-5-APDB H2 H2 H CH2CH(NH2)CH3 OCH3 H
6-APB H H H H CH2CH(NH2)CH3 H
6-APDB H2 H2 H H CH2CH(NH2)CH3 H
6-MAPB H H H H CH2CH(NHCH3)CH3 H
6-MAPDB H2 H2 H H CH2CH(NHCH3)CH3 H
βk-6-MAPB H H H H COCH(NHCH3)CH3 H
6-EAPB H H H H CH2CH(NHCH2CH3)CH3 H
6-EAPDB H2 H2 H H CH2CH(NHCH2CH3)CH3 H
6-MBPB H H H H CH2CH(NHCH3)CH2CH3 H
F-2 HCH3 H2 H OCH3 CH2CH(NH2)CH3 H
F-22 (CH3)2 H2 H OCH3 CH2CH(NH2)CH3 H
7-APB H H H H H CH2CH(NH2)CH3
DOI-2-hemifly H2 H2 I OCH3 H CH2CH(NH2)CH3

See also