Chemistry:2,5-Dimethoxy-4-fluoroamphetamine

2,5-Dimethoxy-4-fluoroamphetamine
Clinical data
Routes of; administration	Oral, Insufflation
ATC code	none;
Legal status
Legal status	CA: Schedule I ; UK: Class A ;
Identifiers
	IUPAC name 1-(4-Fluoro-2,5-dimethoxyphenyl)propan-2-amine;
CAS Number	125903-69-7 ;
PubChem CID	23844155;
ChemSpider	23108678 ;
UNII	93WSW5GYR6;
ChEMBL	ChEMBL267526 ;
Chemical and physical data
Formula	C11H16FNO2
Molar mass	213.252 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CC(Cc1cc(c(cc1OC)F)OC)N;
	InChI InChI=1S/C11H16FNO2/c1-7(13)4-8-5-11(15-3)9(12)6-10(8)14-2/h5-7H,4,13H2,1-3H3 ; Key:NRANUECGGQVXOT-UHFFFAOYSA-N ;
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Short description: Chemical compound

2,5-Dimethoxy-4-fluoroamphetamine (DOF) is a psychedelic drug of the phenethylamine and amphetamine classes. Alexander Shulgin briefly describes DOF in his book PiHKAL:^[1]

Animal studies that have compared DOF to the highly potent DOI and DOB imply that the human activity will be some four to six times less than these two heavier halide analogues.^[2]
– Alexander Shulgin, (PiHKAL)

DOF showed some stimulating effects in humans, but no psychedelic activity, after three doses of 6 mg spaced by one hour.^[3] Researcher Daniel Trachsel further suspected that the molar refraction of the important 4-substituent in DOF and 2C-F may be too low to activate the 5-HT_2A receptor sufficiently.^[4] DOF more closely mimics the effects of the 4-unsubstituted 2,5-dimethoxyamphetamine than the effects of DOC, DOB, and DOI.^[5]^[6]^[7]

References

↑ PiHKAL: A Chemical Love Story. United States: Transform Press. September 1991. pp. 978. ISBN 978-0-9630096-0-9. http://www.erowid.org/library/books_online/pihkal/pihkal.shtml.
↑ "Behavioral and serotonin receptor properties of 4-substituted derivatives of the hallucinogen 1-(2,5-dimethoxyphenyl)-2-aminopropane". Journal of Medicinal Chemistry 25 (10): 1163–1168. October 1982. doi:10.1021/jm00352a013. PMID 7143352.
↑ Biochemistry and Physiology of Substance Abuse, Vol. III. Boca Raton, Florida: CRC Press. 1991.
↑ "Fluorine in psychedelic phenethylamines". Drug Testing and Analysis 4 (7–8): 577–590. July 2012. doi:10.1002/dta.413. PMID 22374819.
↑ "1-(2,5-Dimethoxy-4-(trifluoromethyl)phenyl)-2-aminopropane: a potent serotonin 5-HT2A/2C agonist". Journal of Medicinal Chemistry 37 (25): 4346–4351. December 1994. doi:10.1021/jm00051a011. PMID 7996545.
↑ "Discriminative stimulus properties of hallucinogens and related designer drugs". NIDA Research Monograph 116 (116): 25–44. 1991. PMID 1369672. http://archives.drugabuse.gov/pdf/monographs/download116.html. Retrieved 2015-06-29.
↑ "Binding to the serotonin 5-HT2 receptor by the enantiomers of 125I-DOI". Neuropharmacology 26 (12): 1803–1806. December 1987. doi:10.1016/0028-3908(87)90138-9. PMID 3437942.

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Original source: https://en.wikipedia.org/wiki/2,5-Dimethoxy-4-fluoroamphetamine. Read more

[PiHKAL-1] PiHKAL: A Chemical Love Story. United States: Transform Press. September 1991. pp. 978. ISBN 978-0-9630096-0-9. http://www.erowid.org/library/books_online/pihkal/pihkal.shtml.

[pmid7143352-2] "Behavioral and serotonin receptor properties of 4-substituted derivatives of the hallucinogen 1-(2,5-dimethoxyphenyl)-2-aminopropane". Journal of Medicinal Chemistry 25 (10): 1163–1168. October 1982. doi:10.1021/jm00352a013. PMID 7143352.

[3] Biochemistry and Physiology of Substance Abuse, Vol. III. Boca Raton, Florida: CRC Press. 1991.

[4] "Fluorine in psychedelic phenethylamines". Drug Testing and Analysis 4 (7–8): 577–590. July 2012. doi:10.1002/dta.413. PMID 22374819.

[5] "1-(2,5-Dimethoxy-4-(trifluoromethyl)phenyl)-2-aminopropane: a potent serotonin 5-HT2A/2C agonist". Journal of Medicinal Chemistry 37 (25): 4346–4351. December 1994. doi:10.1021/jm00051a011. PMID 7996545.

[6] "Discriminative stimulus properties of hallucinogens and related designer drugs". NIDA Research Monograph 116 (116): 25–44. 1991. PMID 1369672. http://archives.drugabuse.gov/pdf/monographs/download116.html. Retrieved 2015-06-29.

[7] "Binding to the serotonin 5-HT2 receptor by the enantiomers of 125I-DOI". Neuropharmacology 26 (12): 1803–1806. December 1987. doi:10.1016/0028-3908(87)90138-9. PMID 3437942.

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v t e Phenethylamines
Phenethylamines	Psychedelics: 25B-NBOMe 25C-NBOMe 25D-NBOMe 25I-NBOMe 25N-NBOMe 2C-B 2C-B-AN 2C-Bn 2C-Bu 2C-C 2C-CN 2C-CP 2C-D 2C-E 2C-EF 2C-F 2C-G 2C-G-1 2C-G-2 2C-G-3 2C-G-4 2C-G-5 2C-G-6 2C-G-N 2C-H 2C-I 2C-iP 2C-N 2C-NH2 2C-O 2C-O-4 2C-P 2C-Ph 2C-SE 2C-T 2C-T-2 2C-T-3 2C-T-4 2C-T-5 2C-T-6 2C-T-7 2C-T-8 2C-T-9 2C-T-10 2C-T-11 2C-T-12 2C-T-13 2C-T-14 2C-T-15 2C-T-16 2C-T-17 2C-T-18 2C-T-19 2C-T-20 2C-T-21 2C-T-22 2C-T-22.5 2C-T-23 2C-T-24 2C-T-25 2C-T-27 2C-T-28 2C-T-30 2C-T-31 2C-T-32 2C-T-33 2C-TFE 2C-TFM 2C-YN 2C-V Allylescaline DESOXY Escaline Isoproscaline Jimscaline Macromerine MEPEA Mescaline Metaescaline Methallylescaline Proscaline Psi-2C-T-4 TCB-2 Stimulants: Phenylethanolamine Hordenine Phenethylamine α-Methylphenethylamine (amphetamine) β-Methylphenethylamine m-Methylphenethylamine N-Methylphenethylamine o-Methylphenethylamine p-Methylphenethylamine Methylphenidate Entactogens: Lophophine MDPEA MDMPEA Others: BOH DMPEA
Amphetamines	Psychedelics: 3C-BZ 3C-E 3C-P Aleph Beatrice Bromo-DragonFLY D-Deprenyl DMA DMCPA DMMDA DOB DOC DOEF DOET DOI DOM DON DOPR DOTFM Ganesha MMDA MMDA-2 Psi-DOM TMA TeMA Stimulants: 2-FA 2-FMA 3-FA 3-FMA Acridorex Alfetamine Amfecloral Amfepentorex Amphetamine (Dextroamphetamine, Levoamphetamine) Amphetaminil Benfluorex Benzphetamine Cathine Clobenzorex Dimethylamphetamine Ephedrine Etilamfetamine Fencamfamin Fencamine Fenethylline Fenfluramine (Dexfenfluramine, Levofenfluramine) Fenproporex Flucetorex Fludorex Formetorex Furfenorex Gepefrine 4-Hydroxyamphetamine Iofetamine Isopropylamphetamine Lefetamine Lisdexamfetamine Mefenorex Metaraminol Methamphetamine (Dextromethamphetamine, Levomethamphetamine) Methoxyphenamine MMA Morforex Norfenfluramine L -Norpseudoephedrine N,alpha-Diethylphenylethylamine Oxifentorex Oxilofrine Ortetamine PBA PCA Phenpromethamine PFA PFMA PIA PMA PMEA PMMA Phenylpropanolamine Pholedrine Prenylamine Propylamphetamine Pseudoephedrine Sibutramine Tiflorex Tranylcypromine Xylopropamine Zylofuramine Entactogens: 4-FA 4-FMA 4-MA 4-MMA 4-MTA 5-APB 5-APDB 5-EAPB 5-IT 5-MAPB 5-MAPDB 6-APB 6-APDB 6-Chloro-MDMA 6-EAPB 6-IT 6-MAPB 6-MAPDB EDA IAP 2,3-MDA 3,4-MDA (tenamfetamine) MDEA MDHMA MDMA (midomafetamine) MDOH Methamnetamine MMDMA Naphthylaminopropane TAP Others: 3,4-DCA Amiflamine DiFMDA Selegiline (also D -Deprenyl)
Phentermines	Stimulants: Chlorphentermine Cloforex Clortermine Etolorex Mephentermine Pentorex Phentermine Entactogens: MDPH MDMPH Others: Cericlamine
Cathinones	Stimulants: 3-FMC 4-MC 4-BMC 4-CMC 4-EMC 4-FMC 4-MEC 4-MeMABP 4-MPD Amfepramone Benzedrone Brephedrone Buphedrone Bupropion Cathinone Dimethylcathinone Ethcathinone Eutylone Hydroxybupropion Methcathinone Methedrone NEB N-Ethylhexedrone N-Ethylpentedrone Pentedrone Pentylone Radafaxine Entactogens: 3,4-DMMC 3-MMC Butylone Ethylone Methylone Methylenedioxycathinone Mephedrone
Phenylisobutylamines	Entactogens: 4-CAB 4-MAB Ariadne BDB Butylone EBDB Eutylone MBDB Stimulants: Phenylisobutylamine
Phenylalkylpyrrolidines	Stimulants: α-PBP α-PHP α-PPP α-PVP MDPBP MDPPP MDPV 4-MePBP 4-MePHP 4-MePPP MOPPP MOPVP MPBP MPHP MPPP Naphyrone PEP Prolintane Pyrovalerone
Catecholamines (and close relatives)	6-FNE 6-OHDA a-Me-DA a-Me-TRA Adrenochrome Ciladopa D -DOPA (Dextrodopa) Dimetofrine Dopamine Epinephrine Epinine Etilefrine Ethylnorepinephrine Fenclonine Ibopamine Isoprenaline Isoetarine L -DOPA (Levodopa) L -DOPS (Droxidopa) L -Phenylalanine L -Tyrosine m-Tyramine Metanephrine Metaraminol Metaterol Metirosine Methyldopa N,N-Dimethyldopamine Nordefrin (Levonordefrin) Norepinephrine Norfenefrine (m-Octopamine) Normetanephrine Orciprenaline p-Octopamine p-Tyramine Phenylephrine Synephrine
Miscellaneous	AL-LAD Amidephrine Arbutamine Cafedrine Denopamine Desvenlafaxine Diphenidine Dizocilpine Dobutamine Dopexamine Ephenidine Etafedrine ETH-LAD Famprofazone Fluorolintane Hexapradol IP-LAD Lysergic acid amide Lysergic acid 2-butyl amide Lysergic acid 2,4-dimethylazetidide Lysergic acid diethylamide Methoxamine Methoxphenidine MT-45 PARGY-LAD Phenibut PRO-LAD Pronethalol Salbutamol (Levosalbutamol) Solriamfetol Theodrenaline Thiamphenicol UWA-101

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Chemistry:2,5-Dimethoxy-4-fluoroamphetamine

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Clinical data

Routes of administration	Oral, Insufflation
ATC code	none
Legal status
Legal status	CA: Schedule I UK: Class A
Identifiers
IUPAC name 1-(4-Fluoro-2,5-dimethoxyphenyl)propan-2-amine
CAS Number	125903-69-7^N
PubChem CID	23844155
ChemSpider	23108678^Y
UNII	93WSW5GYR6
ChEMBL	ChEMBL267526^Y
Chemical and physical data
Formula	C₁₁H₁₆FNO₂
Molar mass	213.252 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES CC(Cc1cc(c(cc1OC)F)OC)N
InChI InChI=1S/C11H16FNO2/c1-7(13)4-8-5-11(15-3)9(12)6-10(8)14-2/h5-7H,4,13H2,1-3H3^Y Key:NRANUECGGQVXOT-UHFFFAOYSA-N^Y
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Chemistry:2,5-Dimethoxy-4-fluoroamphetamine

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