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					Chemical compound
Pharmaceutical compound
2C-T-21.5 
2-[4-(3,3-difluoropropylsulfanyl)-2,5-dimethoxyphenyl]ethanamine
 CAS Number PubChem  CID Formula C 12 H 17 F 2 N O 2 S Molar mass −1 3D model (JSmol ) 
COC1=CC(=C(C=C1CCN)OC)SCC(F)F
 
InChI=1S/C12H17F2NO2S/c1-16-9-6-11(18-7-12(13)14)10(17-2)5-8(9)3-4-15/h5-6,12H,3-4,7,15H2,1-2H3
Key:LVCSIKISADNGMR-UHFFFAOYSA-N
 
2C-T-21.5 , also known as 4-(2,2-difluoroethylthio)-2,5-dimethoxyphenethylamine , is a lesser-known psychedelic drug  related to compounds such as 2C-T-21  and 2C-T-28 . It was originally named by Alexander Shulgin  and discussed in his book PiHKAL ,[ 1] Daniel Trachsel  some years later. It has a binding affinity  of 146 nM at 5-HT2A   and 55 nM at 5-HT2C  . It produces typical psychedelic  effects, being slightly less potent but somewhat longer acting than 2C-T-2  or 2C-T-21,[ 2] [ 3] [ 4] fluoroacetate  as a metabolite, instead producing the less toxic difluoroacetic acid .[ 5] [ 6] 
^ Alexander Shulgin. "2C-T-21". PiHKAL  ^ Trachsel D (2012). "Fluorine in psychedelic phenethylamines". Drug Testing and Analysis . 4  (7– 8): 577– 590. doi :10.1002/dta.413 . PMID  22374819 . ^ Luethi D, Trachsel D, Hoener MC, Liechti ME (May 2018). "Monoamine receptor interaction profiles of 4-thio-substituted phenethylamines (2C-T drugs)"  (PDF) . Neuropharmacology . 134  (Pt A): 141– 148. doi :10.1016/j.neuropharm.2017.07.012 . PMID  28720478 . ^ Halberstadt AL, Luethi D, Hoener MC, Trachsel D, Brandt SD, Liechti ME (January 2023). "Use of the head-twitch response to investigate the structure-activity relationships of 4-thio-substituted 2,5-dimethoxyphenylalkylamines" . Psychopharmacology . 240  (1): 115– 126. doi :10.1007/s00213-022-06279-2 . PMC  9816194 PMID  36477925 . ^ Trachsel D, Lehmann D, Enzensperger C (2013). Phenethylamine: Von der Struktur zur Funktion . Nachtschatten Verlag AG. pp. 789– 791. ISBN  978-3-03788-700-4  ^ WO 2023/156450 , Nivorozhkin A, Hartsel JA, Canal CE, Salituro FG, Mueller TA, Greene BJ, Belser A, Avery KL, Reichelt AC, Varty GB, Palfreyman M, "Therapeutic phenethylamine compositions and methods of use.", published 24 August 2023,  assigned to Cybin Irl Ltd.    
No ring subs. 4-Hydroxytryptamines 5-Hydroxytryptamines 5-Methoxytryptamines Other ring subs. 
2,N ,N -TMT 4,N ,N -TMT 5-Bromo-DMT 5-Chloro-DMT 5-Fluoro-DMT 5-N ,N -TMT 7,N ,N -TMT 5-MeO-2,N ,N -TMT 5-MeO-4,N ,N -TMT 6-Fluoro-DMT Bretisilocin (GM-2505; 5-fluoro-MET)  α-Alkyltryptamines 
5-Methoxy-α-alkyltryptamines:  5-MeO-AET α,N ,N -TMT (α-Me-DMT; Alpha-N) 5-MeO-AMT (α,O -DMS; Alpha-O) α,N ,O -TMS (5-MeO-α,N -DMT) α,N ,N ,O -TeMS (5-MeO-α,N ,N -TMT)  Others 
Ergolines /lysergamides  (e.g., LSD )β-Carbolines  and Harmala  alkaloidsharmine , harmaline , 6-methoxyharmalan )Iboga  alkaloids18-MAC , 18-MC , coronaridine , ibogaine , ibogamine , ME-18-MC , noribogaine , tabernanthine , voacangine )Ibogalogs  (e.g., ibogainalog )O -MethylnordehydrobufoteninePartial ergolines  (e.g., NDTDI , RU-28306 , CT-5252 )Piperidinylethylindoles  (e.g., pip-T )Pyrrolidinylethylindoles  (e.g., pyr-T , 5-MeO-pyr-T )Pyrrolidinylmethylindoles  (e.g., MPMI , 4-HO-MPMI (lucigenol) , 5-MeO-MPMI )Tetrahydropyridinylindoles  (e.g., RU-28253 (5-MeO-THPI) , NEtPhOH-THPI ) 
Benzofurans  (e.g., 5-MeO-DiBF , dimemebfe (5-MeO-BFE) , mebfap )Benzothiophenes  (e.g., 3-APBT )Indazolethylamines  (e.g., AL-38022A , O -methyl-AL-34662Indenylethylamines  (e.g., C-DMT )Isotryptamines  (e.g., 6-MeO-isoDMT , Ro60-0175 )MYCO-005 Quinolinylethylamines  (e.g., mefloquine ) 
Others:  2C-B-AN 2C-DB 2C-G-x  (e.g., 2C-G-3 , 2C-G-5 )β-Keto-2C-B (βk-2C-B) β-Keto-2C-I (βk-2C-I) β-Methyl-2C-B (BMB) BOB , BOD , BOH-2C-B )HOT-2 , HOT-7 , HOT-17 )N -Ethyl-2C-B2CD-2-ETO , 2CD-5-ETO , 2CE-5-ETO , 2CE-5iPrO , 2CT2-5-ETO , ASR-2001 (2CB-5PrO) ) Others 
2-TOET 2-TOM 25B-NAcPip 4-HA 5-TOET 5-TOM Benzofurans  (e.g., 5-APB , 5-APDB , 6-APB , 6-APDB , F , F-2 , F-22 )Benzothiophenes  (e.g., 5-APBT , 6-APBT )CT-5172 DMAs  (e.g., 2,4-DMA , 3,4-DMA )Fenfluramine MMA (3-MeO-4-MA) Norfenfluramine 25D-NM-NDEAOP , DOB-NDEPA , DOI-NDEPA , DOM-NDEPA , DOTFM-NDEPA , M-NDEPA , TMA-2-NDEPA )PMA (4-MA) TMA-3 , TMA-4 , TMA-5 )TOMSO ZDCM-04  
1-Aminomethylindanes  (e.g., 2CB-Ind , jimscaline )2-Aminoindanes  (e.g., DOM-AI )3-Benzazepines  (e.g., lorcaserin )3-Phenylpiperidines  (e.g., LPH-5 , LPH-48 )Benzocyclobutenes  (e.g., 2CBCB-NBOMe , TCB-2 , tomscaline )Benzoxepins  (e.g., BBOX , IBOX , TFMBOX )DMBMPP (juncosamine) Ergolines /lysergamides  (e.g., LSD )Glaucine Partial ergolines  (e.g., NDTDI , DEIMDHPCA , DEMPDHPCA , DEMTMPDHPCA , DEMNDHPCA )Phenylcyclopropylamines  (e.g., DMCPA , TMT )Phenyloxazolamines  (aminorexes ) (e.g., 2C-B-aminorex )Pyridopyrroloquinoxalines  (e.g., IHCH-7113 )Z3517967757 ZC-B  
Others 
Arylpiperazines  (e.g., 2C-B-PP , 2-NP , mCPP , MK-212 , ORG-12962 , pCPP , pFPP , quipazine , TFMPP )Dihydrobenzoxazines  (e.g., efavirenz )Phenoxyethylamines  (e.g., CT-4719 , ORG-37684 )Pyridopyrroloquinoxalines  (e.g., IHCH-7113 )Quinazolinylethylamines  (e.g., RH-34 ) Natural sources 
Tryptamines:  Acacia  spp.Acacia acuminata Acacia confusa Ayahuasca  and vinho de Jurema  (e.g., Psychotria viridis  (chacruna)Dipolopterys cabrerana  (chaliponga, chacruna)Mimosa tenuiflora  (Mimosa hostilis ; jurema)Brosimum Brosimum acutifolium  (takini)Hallucinogenic snuffs  (e.g., Anadenanthera peregrina  (yopo, jopo, cohoba, parica, ebene)Anadenanthera colubrina  (vilca, cebil)Incilius alvarius  (Bufo alvarius ; Colorado River toad, Sonoran Desert toad; bufo)Psilocybin-containing mushrooms (magic mushrooms, shrooms)  (e.g., Psilocybe cubensis Psilocybe mexicana  (teonanacatl)Lysergamides:  Achnatherum robustum  (sleepy grass)Epichloë  spp.Ergot (Claviceps )  (e.g., Claviceps purpurea Claviceps paspali Morning glory (Convolvulaceae) seeds  (e.g., Ipomoea tricolor  (tlitliltzin, badoh negro; Ipomoea violacea )Ipomoea corymbosa  (coaxihuitl, ololiúqui; Rivea Corymbosa , Turbina Corymbosa )Argyreia nervosa  (Hawaiian baby woodrose; HBWR)Periglandula  spp.Periglandula ipomoeae Periglandula clandestina