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Substituted benzofurans: Difference between revisions

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[[File:Benzofuran.png|170px|thumbnail|The benzofuran molecule]]
[[File:Substituted_benzofuran.svg|thumb|right|299px||Generic structure of a benzofuran class molecule]]
[[File:SBenzofuran.png|thumb|right|170px||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]], 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.
'''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 ==
== List of benzofuran compounds ==
{| class="wikitable"
{| class="wikitable"
|-
|-
Line 16: Line 15:
! scope="col" | '''Structure'''
! scope="col" | '''Structure'''
|-
|-
| 2-APB || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || H || H || H || H || [[File:2-APB.png|170px]]
| Benzofuran || H || H || H || H || H || H || [[File:Benzofuran.svg|130px]]
|-
|-
| 2-MAPB || CH<sub>2</sub>CH(NHCH<sub>3</sub>)CH<sub>3</sub> || H || H || H || H || H || [[File:2-MAPB.png|170px]]
| 2-APB || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || H || H || H || H || [[File:2-APB.svg|170px]]
|-
|-
| 2-EAPB || CH<sub>2</sub>CH(NHCH<sub>2</sub>CH<sub>3</sub>)CH<sub>3</sub> || H || H || H || H || H || [[File:2-EAPB.png|170px]]
| 2-MAPB || CH<sub>2</sub>CH(NHCH<sub>3</sub>)CH<sub>3</sub> || H || H || H || H || H || [[File:2-MAPB.svg|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]]
| 2-EAPB || CH<sub>2</sub>CH(NHCH<sub>2</sub>CH<sub>3</sub>)CH<sub>3</sub> || H || H || H || H || H || [[File:2-EAPB.svg|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]]
| 3-APB || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || H || H || H || [[File:3-APB.svg|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]]
| Mebfap || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || OCH<sub>3</sub> || H || H || [[File:Mebfap.svg|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-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.svg|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-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.svg|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]]
| 4-APB || H || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || H || H || [[File:4-APB.svg|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]]
| DOB-5-hemifly || 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:DOB-5-hemifly.svg|170px]]
|-
|-
| 5-APDB || H<sub>2</sub> || H<sub>2</sub> || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || H || [[File:5-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.svg|170px]]
|-
|-
| 5-MAPB || H || H || H || CH<sub>2</sub>CH(NHCH<sub>3</sub>)CH<sub>3</sub> || H || H || [[File:5-MAPB.png|170px]]
| 5-APDB || H<sub>2</sub> || H<sub>2</sub> || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || H || [[File:5-APDB.svg|170px]]
|-
|-
| 5-MAPDB || H<sub>2</sub> || H<sub>2</sub> || H || CH<sub>2</sub>CH(NHCH<sub>3</sub>)CH<sub>3</sub> || H || H || [[File:5-MAPDB.png|170px]]
| [[5-MAPB]] || H || H || H || CH<sub>2</sub>CH(NHCH<sub>3</sub>)CH<sub>3</sub> || H || H || [[File:5-MAPB.svg|170px]]
|-
|-
| bk-5-MAPB || H || H || H || COCH(NHCH<sub>3</sub>)CH<sub>3</sub> || H || H || [[File:bk-5-MAPB.png|170px]]
| 5-MAPDB || H<sub>2</sub> || H<sub>2</sub> || H || CH<sub>2</sub>CH(NHCH<sub>3</sub>)CH<sub>3</sub> || H || H || [[File:5-MAPDB.svg|170px]]
|-
|-
| 5-EAPB || H || H || H || CH<sub>2</sub>CH(NHCH<sub>2</sub>CH<sub>3</sub>)CH<sub>3</sub> || H || H || [[File:5-EAPB.png|170px]]
| βk-5-MAPB || H || H || H || COCH(NHCH<sub>3</sub>)CH<sub>3</sub> || H || H || [[File:βk-5-MAPB.svg|170px]]
|-
|-
| 5-EAPDB || H<sub>2</sub> || H<sub>2</sub> || H || CH<sub>2</sub>CH(NHCH<sub>2</sub>CH<sub>3</sub>)CH<sub>3</sub> || H || H || [[File:5-EAPDB.png|170px]]
| 5-EAPB || H || H || H || CH<sub>2</sub>CH(NHCH<sub>2</sub>CH<sub>3</sub>)CH<sub>3</sub> || H || H || [[File:5-EAPB.svg|170px]]
|-
|-
| 5-MBPB || H || H || H || CH<sub>2</sub>CH(NHCH<sub>3</sub>)CH<sub>2</sub>CH<sub>3</sub> || H || H || [[File:5-MBPB.png|170px]]
| 5-EAPDB || H<sub>2</sub> || H<sub>2</sub> || H || CH<sub>2</sub>CH(NHCH<sub>2</sub>CH<sub>3</sub>)CH<sub>3</sub> || H || H || [[File:5-EAPDB.svg|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]]
| 5-MBPB || H || H || H || CH<sub>2</sub>CH(NHCH<sub>3</sub>)CH<sub>2</sub>CH<sub>3</sub> || H || H || [[File:5-MBPB.svg|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]]
| 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.svg|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-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.svg|170px]]
|-
|-
| 6-APDB || H<sub>2</sub> || H<sub>2</sub> || H || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || [[File:6-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.svg|170px]]
|-
|-
| 6-MAPB || H || H || H || H || CH<sub>2</sub>CH(NHCH<sub>3</sub>)CH<sub>3</sub> || H || [[File:6-MAPB.png|170px]]
| [[6-APDB]] || H<sub>2</sub> || H<sub>2</sub> || H || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || [[File:6-APDB.svg|170px]]
|-
|-
| 6-MAPDB || H<sub>2</sub> || H<sub>2</sub> || H || H || CH<sub>2</sub>CH(NHCH<sub>3</sub>)CH<sub>3</sub> || H || [[File:6-MAPDB.png|170px]]
| 6-MAPB || H || H || H || H || CH<sub>2</sub>CH(NHCH<sub>3</sub>)CH<sub>3</sub> || H || [[File:6-MAPB.svg|170px]]
|-
|-
| bk-6-MAPB || H || H || H || H || COCH(NHCH<sub>3</sub>)CH<sub>3</sub> || H || [[File:bk-6-MAPB.png|170px]]
| 6-MAPDB || H<sub>2</sub> || H<sub>2</sub> || H || H || CH<sub>2</sub>CH(NHCH<sub>3</sub>)CH<sub>3</sub> || H || [[File:6-MAPDB.svg|170px]]
|-
|-
| 6-EAPB || H || H || H || H || CH<sub>2</sub>CH(NHCH<sub>2</sub>CH<sub>3</sub>)CH<sub>3</sub> || H || [[File:6-EAPB.png|170px]]
| βk-6-MAPB || H || H || H || H || COCH(NHCH<sub>3</sub>)CH<sub>3</sub> || H || [[File:βk-6-MAPB.svg|170px]]
|-
|-
| 6-EAPDB || H<sub>2</sub> || H<sub>2</sub> || H || H || CH<sub>2</sub>CH(NHCH<sub>2</sub>CH<sub>3</sub>)CH<sub>3</sub> || H || [[File:6-EAPDB.png|170px]]
| 6-EAPB || H || H || H || H || CH<sub>2</sub>CH(NHCH<sub>2</sub>CH<sub>3</sub>)CH<sub>3</sub> || H || [[File:6-EAPB.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.png|170px]]
| 6-EAPDB || H<sub>2</sub> || H<sub>2</sub> || H || H || CH<sub>2</sub>CH(NHCH<sub>2</sub>CH<sub>3</sub>)CH<sub>3</sub> || H || [[File:6-EAPDB.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.png|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-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.png|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]]
|-
|-
| 7-APB || H || H || H || H || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || [[File:7-APB.png|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]]
|-
|-
| 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]]
| 7-APB || H || H || H || H || H || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || [[File:7-APB.svg|170px]]
|-
| DOI-2-hemifly || 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:DOI-2-hemifly.svg|170px]]
|-
| [[Bromo-DragonFLY]] || H || H || Br || O- || CH=CH- || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || [[File:Bromo-DragonFLY.svg|170px]]
|-
| [[2C-B-FLY]] || H<sub>2</sub> || H<sub>2</sub> || Br || OCH<sub>2</sub>- || CH<sub>2</sub>- || CH<sub>2</sub>CH<sub>2</sub>NH<sub>2</sub> || [[File:2C-B-FLY.svg|170px]]
|-
| [[Tasimelteon]] || H<sub>2</sub> || H<sub>2</sub> || C<sub>3</sub>H<sub>4</sub>CH<sub>2</sub>NHCOCH<sub>2</sub>CH<sub>3</sub> || H || H || H || [[File:Tasimelteon.svg|170px]]
|-
| [[Ramelteon]] || H<sub>2</sub> || H<sub>2</sub> || CH(CH<sub>2</sub>-)CH<sub>2</sub>CH<sub>2</sub>NHCOCH<sub>2</sub>CH<sub>3</sub> || CH<sub>2</sub>- || H || H || [[File:Ramelteon.svg|170px]]
|-
| [[Vilazodone]] || CONH<sub>2</sub> || H || H || C<sub>4</sub>H<sub>8</sub>N<sub>2</sub>(CH<sub>2</sub>)<sub>4</sub>C<sub>9</sub>H<sub>5</sub>N<sub>2</sub> || H || H || [[File:Vilazodone.svg|230px]]
|-
|-
|}
|}
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*[[Entactogen]]
*[[Entactogen]]
*[[Phenethylamines]]
*[[Phenethylamines]]
==External links==
* [https://en.wikipedia.org/wiki/Substituted_benzofuran Substituted benzofuran (Wikipedia)]
[[Category:Chemical class]]
[[Category:Benzofuran| ]]

Latest revision as of 01:19, 4 October 2021

This article is a stub.

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

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
Benzofuran H H H H H H
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
Bromo-DragonFLY H H Br O- CH=CH- CH2CH(NH2)CH3
2C-B-FLY H2 H2 Br OCH2- CH2- CH2CH2NH2
Tasimelteon H2 H2 C3H4CH2NHCOCH2CH3 H H H
Ramelteon H2 H2 CH(CH2-)CH2CH2NHCOCH2CH3 CH2- H H
Vilazodone CONH2 H H C4H8N2(CH2)4C9H5N2 H H

See also

Retrieved from "http://psy.st/w/index.php?title=Substituted_benzofurans&oldid=124705"