Buy 2C-B-FLY Online; aka: 8-bromo-2,3,6,7-benzo-dihydro-difuran-ethylamine or 2-(8-bromo-2,3,6,7-tetrahydrofuro[2,3-f] benzofuran-4-yl)ethanamine.
A set of phenethylamine derivatives referred to as the FLY compounds, named for their insect-like look of “wing-like” furan or dihydrofuran rings fused on the other sides of the relevant benzene ring, have been diagnosed with allegedly effective hallucinogenic results.1 2C-B-fly is the dihydrodifuran analog of the schedule I hallucinogen 4-bromo-2,5-dimethoxyphenethylamine (2C-B).1,2 it’s far expected to reveal comparable activity to 2C-B, which acts as a partial agonist on the five-HT2A serotonin receptor and demonstrates excessive binding affinity for the five-HT2B and 5-HT2C serotonin receptors.3,four This product is intended for forensic and studies purposes.
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In idea, dihydrodifuran analogues of any of the 2Cx / DOx own family of medication can be made, and might be anticipated to reveal similar pastime to the decide compound. So inside the equal way that 2C-B-FLY is the dihydrodifuran analogue of 2C-B, the 8-iodo equal 2C-I-FLY would be the dihydrodifuran analogue of 2C-I, and the eight-methyl equivalent 2C-D-FLY would be the dihydrodifuran analogue of 2C-D.
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RESEARCH ONLY! NOT FOR HUMAN CONSUMPTION..
PRODUCT DESCRIPTION REFERENCES
1. Reed, E.C., and Kiddon, G.S. The characterization of three fly compounds (2C-B-FLY, 3C-B-FLY, and Bromo-Dragon FLY). DEA Microgram Journal 5(1-4), 1-8 (2007).
2. Pichini, S., Pujadas, M., Marchei, E., et al. Liquid chromatography-atmospheric pressure ionization electrospray mass spectrometry determination of “hallucinogenic designer drugs” in urine of consumers. Journal of Pharmaceutical & Biomedical Analysis 47(2), 335-342 (2008).
3. Monte, A.P., Marona-Lewicka, D., Parker, M.A., et al. Dihydrobenzofuran analogues of hallucinogens. 3. Models of 4-substituted (2,5-dimethoxyphenyl)alkylamine derivatives with rigidified methoxy groups. Journal of Medicinal Chemistry 39, 2953-2961 (1996).
4. Chambers, J.J., Kurrasch-Orbaugh, D.M., Parker, M.A., et al. Enantiospecific synthesis and pharmacological evaluation of a series of super-potent, conformationally restricted 5-HT2A/2C receptor agonists. Journal of Medicinal Chemistry 44, 1003-1010 (2001).
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