HOT-17: Difference between revisions
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Script assisted update of identifiers from ChemSpider, CommonChemistry and FDA for the Chem/Drugbox validation project - Updated: InChI1 InChIKey1 SMILES. |
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| OtherNames = 2-[4-(Isobutylthio)-2,5-dimethoxyphenyl]ethanaminol |
| OtherNames = 2-[4-(Isobutylthio)-2,5-dimethoxyphenyl]ethanaminol |
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| Section1 = {{Chembox Identifiers |
| Section1 = {{Chembox Identifiers |
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| InChI1 = 1/C14H23NO3S/c1-5-10(2)19-14-9-12(17-3)11(6-7-15-16)8-13(14)18-4/h8-10,15-16H,5-7H2,1-4H3 |
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| InChIKey1 = BUKIXGXYEUJJHQ-UHFFFAOYAH |
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| ChemSpiderID=21106319 |
| ChemSpiderID=21106319 |
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| PubChem = |
| PubChem = |
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| SMILES = |
| SMILES = CC(CC)Sc1cc(OC)c(cc1OC)CCNO |
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| Section2 = {{Chembox Properties |
| Section2 = {{Chembox Properties |
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| Formula = C<sub>14</sub>H<sub>23</sub>NO<sub>3</sub>S |
| Formula = C<sub>14</sub>H<sub>23</sub>NO<sub>3</sub>S |
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Revision as of 18:29, 30 October 2010
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| Names | |
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| IUPAC name
N-[2-(4-sec-Butylsulfanyl-2,5-dimethoxy-phenyl)-ethyl]-hydroxylamine
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| Other names
2-[4-(Isobutylthio)-2,5-dimethoxyphenyl]ethanaminol
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
CompTox Dashboard (EPA)
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| Properties | |
| C14H23NO3S | |
| Molar mass | 285.40 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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HOT-17, or 2,5-dimethoxy-4-(β-isobutylthio)-N-hydroxyphenethylamine, is a psychedelic phenethylamine of the 2C family. It was presumably first synthesized by Alexander Shulgin and reported in his book, PiHKAL (Phenethylamines i Have Known And Loved).
Chemistry
HOT-17's full chemical name is 2-[4-(2-isobutylthio)-2,5-dimethoxyphenyl-N-hydroxyethanamine. It has structural properties similar to 2C-T-17 and to other drugs in the HOT- series, with the most closely related compounds being HOT-2 and HOT-7.
General information
The dosage range of HOT-17 is typically 70-120mg and its duration is approximately 12–18 hours according to Shulgin. HOT-17 produces time distortion and general psychedelia. It also has little to no body load.
See also
External links
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