2C-H , or 2,5-dimethoxyphenylethylamine, is a substituted phenethylamine from a 2C family . 2C-H was first synthesized in 1932 by Johanness S. Buck [1] In the book PiHKAL , the dosage and duration of the 2C-H effect are not indicated. Data on human 2C-H testing has not been published, as it is likely to be destroyed by monoamine oxidase before it causes significant psychotropic effects [2] . There is very little data on the pharmacological properties, metabolism and toxicity of 2C-H.
| 2,5-dimethoxyphenylethylamine | |
|---|---|
 | |
| Are common | |
| Systematic name | 2- (2,5-dimethoxyphenyl) ethylamine |
| Abbreviations | 2C-H |
| Chem. formula | C 10 H 15 NO 2 |
| Physical properties | |
| Molar mass | 181.23 g / mol |
| Density | 1,089 g / cm³ |
| Thermal properties | |
| T. melt. | 139 ° C |
| Vapor pressure | 10 (160 ° C) mm Hg |
| Classification | |
| Reg. CAS number | 3600-86-0 |
| Pubchem | |
| Reg. EINECS number | |
| SMILES | |
| Inchi | |
| CHEBI | |
| Chemspider | |
2C-H is used as a precursor in the synthesis of other substituted phenylethylamines .
Sources
- ↑ Buck, Johannes S. Hydroxy- and Dihydroxyphenylethylmethylamines and their Ether (Neopr.) // Journal of Chemical Society. - 1932. - Vol . 54 , No. 9 . - pp . 3661-3665 . - DOI : 10.1021 / ja01348a024 .
- ↑ Alexander Shulgin, Ann Shulgin. 2C-H: Extensions and commentary // PiHKAL: A Chemical Love Story. - Berkeley, California: Transform Press, 1995. - 978 p. - ISBN 0-963-0096-0-5 .