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F-22 (drug)
| Field | Value | |||
|---|---|---|---|---|
| Watchedfields | changed | |||
| verifiedrevid | 399929286 | |||
| drug_name | F-22 | |||
| image | F-22_(psychedelic_drug).svg | |||
| image_class | skin-invert-image | |||
| width | 250px | |||
| routes_of_administration | Oral | |||
| ATC_prefix | None | |||
| duration_of_action | Unknown | |||
| CAS_number_Ref | ||||
| CAS_number | 952016-51-2 | |||
| PubChem | 16051705 | |||
| ChemSpiderID_Ref | ||||
| ChemSpiderID | 13180083 | |||
| UNII_Ref | ||||
| UNII | QS9HMZ85HN | |||
| synonyms | 6-(2-Aminopropyl)-2,2-dimethyl-5-methoxy-2,3-dihydrobenzofuran; Benzofuran-2,2-dimethyl-5-methoxy-6-(2-aminopropane) | |||
| IUPAC_name | 1-(5-methoxy-2,2-dimethyl-2,3-dihydro-1-benzofuran-6-yl)propan-2-amine | |||
| C | 14 | H=21 | N=1 | O=2 |
| SMILES | C1=C2C(=CC(=C1CC(C)N)OC)CC(O2)(C)C | |||
| StdInChI_Ref | ||||
| StdInChI | 1S/C14H21NO2/c1-9(15)5-10-6-13-11(7-12(10)16-4)8-14(2,3)17-13/h6-7,9H,5,8,15H2,1-4H3 | |||
| StdInChIKey_Ref | ||||
| StdInChIKey | ZUGGTXPIKSRFHP-UHFFFAOYSA-N |
| Drugs.com =
| elimination_half-life =
F-22, also known as 6-(2-aminopropyl)-2,2-dimethyl-5-methoxy-2,3-dihydrobenzofuran or as benzofuran-2,2-dimethyl-5-methoxy-6-(2-aminopropane), is a lesser-known psychoactive drug of the amphetamine and benzofuran families. F-22 was first synthesized by Alexander Shulgin. In his book PiHKAL, the minimum dosage is listed as 15 mg, and the duration unknown. F-22 produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of F-22. F-22 is the derivative of 6-APDB with two methyl groups at the carbon 2 and a methoxy group at carbon 5 of the benzofuran core.
Society and culture
Legal status
United Kingdom
This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.
References
References
- {{CitePiHKAL [http://www.erowid.org/library/books_online/pihkal/pihkal080.shtml F-22 Entry]
- "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design.
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