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Chemistry 2C-B-FLY
#1
2C-B-FLY is a substituted molecule of the phenethylamine and dihydrobenzofuran chemical classes. 2C-B-FLY features a phenyl ring bound to an amino (NH2) group through an ethyl chain and contains a bromine atom attached to carbon R4 of the phenyl ring.

It is an atypical psychedelic phenethylamine which is closely analogous to 2C-B; it is the dihydrofuran analog to 2C-B, where it incorporates the methoxy groups bound to R2 and R5 of 2C-B into five-member dihydrofuran rings fused to the central benzene ring.

2C-B-FLY belongs to a group of phenethylamine derivatives referred to as the FLY compounds, named for their insect-like appearance of two “wing-like” tetrahydrofuran rings fused on the opposite sides of the central benzene ring. The incorporation of the two methoxy groups into the 5 member rings fixes them into the optimum position for binding to the receptors they interact with resulting in an increase in potency compared to the compound's non-rigid counterpart 2C-B.
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#2
HISTORY & STATS 02
2C-B was discovered in 1974 by Shulgin. The following year, he described it as “beautifully psychoactive” and compared its effects to mescaline and LSD. He also noted the compound’s empathogenic properties and—as with MDMA—recommended it to a small number of psychotherapists for experimentation with their clients
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#3
Communicating with others may become difficult or confusing, although it can also be easier for some. In any case, empathy and sociability are generally increased. Conceptual thinking, introspective insights, and spiritual ideation are also common—especially when alone. There may be a slight softening of the ego.
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#4
A large number of symmetrical and unsymmetrical derivatives can be produced by using different combinations of ring systems. Because the 2- and 5- positions (using phenethylamine numbering scheme
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