Warning
This is an unofficial archive of PsychonautWiki as of 2025-08-11T15:14:44Z. Content on this page may be outdated, incomplete, or inaccurate. Please refer to the original page for the most up-to-date information.

Substituted benzofurans: Difference between revisions

From PsychonautWiki Archive
Jump to navigation Jump to search
← Older editNewer edit →
>BronzeManul
m Replaced red links with plain text.
>BronzeManul
m Reordered
Line 23: Line 23:
|-
|-
| 3-APB || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || H || H || H || [[File:3-APB.png|170px]]
| 3-APB || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || H || H || H || [[File:3-APB.png|170px]]
|-
| Mebfap || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || OCH<sub>3</sub> || H || H || [[File:Mebfap.png|170px]]
|-
| 5-MeO-BFE || H || CH<sub>2</sub>CH<sub>2</sub>N(CH<sub>3</sub>)<sub>2</sub> || H || OCH<sub>3</sub> || H || H || [[File:5-MeO-BFE.png|170px]]
|-
| [[5-MeO-DiBF]] || H || CH<sub>2</sub>CH<sub>2</sub>N(CH(CH<sub>3</sub>)<sub>2</sub>)<sub>2</sub> || H || OCH<sub>3</sub> || H || H || [[File:5-MeO-DiBF.png|170px]]
|-
|-
| 4-APB || H || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || H || H || [[File:4-APB.png|170px]]
| 4-APB || H || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || H || H || [[File:4-APB.png|170px]]
|-
| 5-MeO-7-Br-4-APDB || H<sub>2</sub> || H<sub>2</sub> || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || OCH<sub>3</sub> || H || Br || [[File:5-MeO-7-Br-4-APDB.png|170px]]
|-
|-
| [[5-APB]] || H || H || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || H || [[File:5-APB.png|170px]]
| [[5-APB]] || H || H || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || H || [[File:5-APB.png|170px]]
Line 44: Line 52:
| 5-DBFPV || H<sub>2</sub> || H<sub>2</sub> || H || COCH(NC<sub>4</sub>H<sub>8</sub>)CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> || H || H || [[File:5-DBFPV.png|170px]]
| 5-DBFPV || H<sub>2</sub> || H<sub>2</sub> || H || COCH(NC<sub>4</sub>H<sub>8</sub>)CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> || H || H || [[File:5-DBFPV.png|170px]]
|-
|-
 
| 6-MeO-5-APDB || H<sub>2</sub> || H<sub>2</sub> || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || OCH<sub>3</sub> || H || [[File:6-MeO-5-APDB.png|170px]]
|-
| [[6-APB]] || H || H || H || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || [[File:6-APB.png|170px]]
| [[6-APB]] || H || H || H || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || [[File:6-APB.png|170px]]
|-
|-
Line 68: Line 77:
|-
|-
| 4-I-5-MeO-7-APDB || H<sub>2</sub> || H<sub>2</sub> || I || OCH<sub>3</sub> || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || [[File:4-I-5-MeO-7-APDB.png|170px]]
| 4-I-5-MeO-7-APDB || H<sub>2</sub> || H<sub>2</sub> || I || OCH<sub>3</sub> || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || [[File:4-I-5-MeO-7-APDB.png|170px]]
|-
| Mebfap || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || OCH<sub>3</sub> || H || H || [[File:Mebfap.png|170px]]
|-
| 5-MeO-BFE || H || CH<sub>2</sub>CH<sub>2</sub>N(CH<sub>3</sub>)<sub>2</sub> || H || OCH<sub>3</sub> || H || H || [[File:5-MeO-BFE.png|170px]]
|-
| [[5-MeO-DiBF]] || H || CH<sub>2</sub>CH<sub>2</sub>N(CH(CH<sub>3</sub>)<sub>2</sub>)<sub>2</sub> || H || OCH<sub>3</sub> || H || H || [[File:5-MeO-DiBF.png|170px]]
|-
| 5-MeO-7-Br-4-APDB || H<sub>2</sub> || H<sub>2</sub> || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || OCH<sub>3</sub> || H || Br || [[File:5-MeO-7-Br-4-APDB.png|170px]]
|-
| 6-MeO-5-APDB || H<sub>2</sub> || H<sub>2</sub> || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || OCH<sub>3</sub> || H || [[File:6-MeO-5-APDB.png|170px]]
|-
|-
|}
|}

Revision as of 23:15, 27 October 2016

This article is a stub.

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

The benzofuran molecule
General formula of a benzofuran class molecule.

Benzofurans are chemical compounds, which contain a benzofuran ring in their structure. Most of the benzofurans are research chemicals and are fairly new to the market. They are most commonly stimulants or entactogens. Benzofuran compounds are often analogues of MDxx and Tryptamine compounds where a benzofuran ring has replaced the 3,4-methylenedioxy benzene 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 File:2-APB2.png
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
5-MeO-7-Br-4-APDB H2 H2 CH2CH(NH2)CH3 OCH3 H Br File:5-MeO-7-Br-4-APDB.png
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
bk-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 File:6-MeO-5-APDB.png
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
bk-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 CH3 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
4-I-5-MeO-7-APDB H2 H2 I OCH3 H CH2CH(NH2)CH3 File:4-I-5-MeO-7-APDB.png

See also

Retrieved from "http://psy.st/w/index.php?title=Substituted_benzofurans&oldid=71758"