6-APB was synthesized by David E. Nichols in 1993 as a potential non-neurotoxic alternative to MDMA. 6-APB is is an entactogen of the benzofuran family. 6-APB is structurally related to other entactogens like MDA, MDMA, 5-APB, and 5-MAPB. Also known as 6-(2-aminopropyl)benzofuran, 6-APB does not contain a methyl substitution on RN. It is composed of an an oxygen-substituted benzofuran ring fused at R3 and R4 of the phenyl ring.

IUPAC: 1-(1-Benzofuran-6-yl)propan-2-amine fumarate


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