25B-NBF

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25B-NBF
25B-NBF.svg
Clinical data
ATC code
  • (HCl): none
Legal status
Legal status
  • DE: NpSG (Industrial and scientific use only)
  • UK: Class A
Identifiers
IUPAC name
  • 2-(4-Bromo-2,5-dimethoxyphenyl)-N-(2-fluorobenzyl)ethanamine
CAS Number
ChemSpider
UNII
Chemical and physical data
3D model (JSmol)
SMILES
  • (HCl): COC1=CC(CCNCC2=CC=CC=C2F)=C(OC)C=C1Br

25B-NBF (2C-B-NBF, NBF-2C-B) is a derivative of the phenethylamine hallucinogen 2C-B, which acts as a highly potent partial agonist for the human 5-HT2A receptor.[1][2]

Legality[]

Sweden[]

The Riksdag added 25B-NBF to Narcotic Drugs Punishments Act under swedish schedule I ("substances, plant materials and fungi which normally do not have medical use") as of January 26, 2016, published by Medical Products Agency (MPA) in regulation HSLF-FS 2015:35 listed as 25B-NBF, and 2-(4-bromo-2,5-dimetoxifenyl)-N-(2-fluorobensyl)etanamin.[3]

United Kingdom[]

This substance is a Class A drug in the United Kingdom as a result of the N-benzylphenethylamine catch-all clause in the Misuse of Drugs Act 1971.[4]


Analogues and derivatives[]

Analogues and derivatives of 2C-B:

:

25-NB:

  • 25B-NB
  • 25B-NBF
  • 25B-NBOH
  • 25B-NBOMe (NBOMe-2CB)

:

Substituted benzofurans:

Other:

  • 2C-B-BUTTERFLY
  • 2CB-Ind
  • βk-2C-B (beta-keto 2C-B)
  • N-Ethyl-2C-B
  • TCB-2 (2C-BCB)

References[]

  1. ^ Hansen M, Phonekeo K, Paine JS, Leth-Petersen S, Begtrup M, Bräuner-Osborne H, Kristensen JL (March 2014). "Synthesis and structure-activity relationships of N-benzyl phenethylamines as 5-HT2A/2C agonists". ACS Chemical Neuroscience. 5 (3): 243–9. doi:10.1021/cn400216u. PMC 3963123. PMID 24397362.
  2. ^ Hansen M (2010-12-16). Design and Synthesis of Selective Serotonin Receptor Agonists for Positron Emission Tomography Imaging of the Brain (Ph.D. thesis). University of Copenhagen. doi:10.13140/RG.2.2.33671.14245.
  3. ^ "Data" (PDF). lakemedelsverket.se. 2015.
  4. ^ "The Misuse of Drugs Act 1971 (Ketamine etc.) (Amendment) Order 2014". www.legislation.gov.uk.
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