| Identification | Back Directory | [Name]
1-(8-Bromo-2,3,6,7-tetrahydrobenzodifuran-4-yl)-2-aminoethane hydrochloride | [CAS]
178557-21-6 | [Synonyms]
2C-B-FLY
2C-B-fly (hydrochloride)
2C-B-FLY or 2c-b-dragonfly
2C-B-FLY hydrochloride solution
DesMethyl-8-broMo Dragonfly Hydrochloride
2-(4-bromo-2,3,6,7-tetrahydrofuro[2,3-f][1]benzofuran-8-yl)ethanamine
2-(8-Bromo-2,3,6,7-tetrahydrobenzo-[1,2-b:4,5-b']difuran-4-yl)ethanamine
1-(8-Bromo-2,3,6,7-tetrahydrobenzodifuran-4-yl)-2-aminoethane hydrochloride
1-(8-bromo-2,3,6,7-tetrahydrobenzo[1,2-b:4,5-b']difuran-4-yl)-2-aminoethane
8-BroMo-2,3,6,7-tetrahydrobenzo[1,2-b:4,5-b']difuran-4-ethanaMine Hydrochloride
2-(8-Bromo-2,3,6,7-tetrahydrobenzofuro[5,6-b]furan-4-yl)ethanamine hydrochloride
Benzo[1,2-b:4,5-b']difuran-4-ethanaMine,8-broMo-2,3,6,7-tetrahydro-, hydrochloride (9CI) | [Molecular Formula]
C12H14BrNO2.ClH | [MDL Number]
MFCD09751142 | [MOL File]
178557-21-6.mol | [Molecular Weight]
320.612 |
| Chemical Properties | Back Directory | [Fp ]
2℃ | [storage temp. ]
-20°C | [solubility ]
DMF: 1 mg/ml; DMSO: 5 mg/ml; DMSO:PBS(pH7.2) (1:1): 0.5 mg/ml; Methanol: 1 mg/ml | [form ]
A crystalline solid |
| Hazard Information | Back Directory | [Description]
A group of phenethylamine derivatives referred to as the FLY compounds, named for their insect-like appearance of two “wing-like” furan or dihydrofuran rings fused on the opposite sides of the central benzene ring, have been identified with allegedly potent hallucinogenic effects. 2C-B-FLY is the dihydrodifuran analog of the Schedule I hallucinogen 4-bromo-2,5-dimethoxyphenethylamine (2C-B). It is expected to show similar activity to 2C-B, which acts as a partial agonist at the 5-HT2A serotonin receptor and demonstrates high binding affinity for the 5-HT2B and 5-HT2C serotonin receptors. This product is intended for forensic and research purposes. | [Uses]
A metabolite of Bromo Dragonfly (B684210). | [References]
[1] De Souza, F.I., Zumiotti, A.V., and Da Silva, C.F. Neuregulins 1-α and 1-β on the regeneration the peripheral nerves[J]. Acta Ortop Bras.
[2] SIMONA PICHINI . Liquid chromatography–atmospheric pressure ionization electrospray mass spectrometry determination of “hallucinogenic designer drugs” in urine of consumers[J]. Journal of pharmaceutical and biomedical analysis, 2008, 47 2: Pages 335-342. DOI: 10.1016/j.jpba.2007.12.039
[3] AARON P. MONTE. Dihydrobenzofuran Analogues of Hallucinogens. 3. 1 Models of 4-Substituted (2,5-Dimethoxyphenyl)alkylamine Derivatives with Rigidified Methoxy Groups 2[J]. Journal of Medicinal Chemistry, 1996, 39 15: 2953-2961. DOI: 10.1021/jm960199j
[4] JAMES J. CHAMBERS. Enantiospecific Synthesis and Pharmacological Evaluation of a Series of Super-Potent, Conformationally Restricted 5-HT2A/2C Receptor Agonists[J]. Journal of Medicinal Chemistry, 2001, 44 6: 1003-1010. DOI: 10.1021/jm000491y |
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