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Substituted benzofurans: Difference between revisions
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! scope="col" | '''Structure''' | ! scope="col" | '''Structure''' | ||
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| 2-APB || CH<sub>2</sub>CH(NH<sub>2</sub>)CH<sub>3</sub> || H || H || H || H || H || [[File:2- | | 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]] | ||
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| 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-MAPB || CH<sub>2</sub>CH(NHCH<sub>3</sub>)CH<sub>3</sub> || H || H || H || H || H || [[File:2-MAPB.png|170px]] |
Revision as of 00:07, 28 October 2016
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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 | ![]() |
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 |