25CN-NBOMe

25CN-NBOMe
Identifiers
	IUPAC name 2,5-Dimethoxy-4-(2-(2-methoxybenzylamino)ethyl)benzonitrile;
CAS Number	1354632-16-8 ;
PubChem CID	152743520;
ChemSpider	58191430 ;
UNII	2B3AN5ZD3X;
Chemical and physical data
Formula	C19H22N2O3
Molar mass	326.396 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES N#CC1=CC(OC)=C(CCNCC2=C(OC)C=CC=C2)C=C1OC;
	InChI InChI=1S/C19H22N2O3/c1-22-17-7-5-4-6-15(17)13-21-9-8-14-10-19(24-3)16(12-20)11-18(14)23-2/h4-7,10-11,21H,8-9,13H2,1-3H3 ; Key:QBJWOIWLBRLGKZ-UHFFFAOYSA-N ;

25CN-NBOMe (2C-CN-NBOMe, NBOMe-2C-CN) is a derivative of the phenethylamine 2C-CN. It acts in a similar manner to related compounds such as 25I-NBOMe, which are potent agonists at the 5HT_2A receptor.^[1]^[2]

Legality

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.^[3]

References

^ 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.
^ 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.
^ "The Misuse of Drugs Act 1971 (Ketamine etc.) (Amendment) Order 2014". UK Statutory Instruments 2014 No. 1106. www.legislation.gov.uk.