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| Clinical data | |
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| Other names | 2,5-Dimethoxy-3,4-(tetramethylene)phenethylamine; 3,4-Tetramethylene-2,5-dimethoxyphenethylamine; 6-(2-Aminoethyl)-5,8-dimethoxytetralin |
| Routes of administration | Unknown [1] |
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| Pharmacokinetic data | |
| Onset of action | Unknown [1] |
| Duration of action | Unknown [1] |
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| Chemical and physical data | |
| Formula | C14H21NO2 |
| Molar mass | 235.327 g·mol−1 |
| 3D model (JSmol) | |
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2C-G-4, also known as 2,5-dimethoxy-3,4-(tetramethylene)phenethylamine or as 6-(2-aminoethyl)-5,8-dimethoxytetralin, is a chemical compound of the phenethylamine and 2C families. [1] It is the derivative of 2C-G (2C-G-0) in which the 3,4-dimethyl groups have been connected via two additional carbon atoms to form a cyclohexane ring attached to the benzene ring and hence has a tetralin (1,2,3,4-tetrahydronaphthalene) ring system. [1] The compound was included by Alexander Shulgin as an entry in his 1991 book PiHKAL (Phenethylamines I Have Known and Loved). [1] However, Shulgin was unable to complete the last step of the chemical synthesis of the compound and never tested it. [1] In any case, he anticipated that it would be an active compound. [1] The synthesis of 2C-G-4 has been described. [1] 2C-G-4 was first described in the literature by Shulgin in PiHKAL in 1991. [1]
