DOI | |
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Salts [] | |
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2,5-Dimethoxy-4-iodoamphetamine hydrochloride | |
Molecular structure via molpic | |
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Molecular formula | C11H16INO2 |
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Molecular mass | 321.15 g/mol |
Predicted LogP | 2.5 |
Chirality | racemic |
Identifiers [] | |
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IUPAC name | 1-(4-iodo-2,5-dimethoxyphenyl)propan-2-amine |
SMILES | CC(CC1=CC(=C(C=C1OC)I)OC)N |
InChI | InChI=1S/C11H16INO2/c1-7(13)4-8-5-11(15-3)9(12)6-10(8)14-2/h5-7H,4,13H2,1-3H3 |
InChIKey | BGMZUEKZENQUJY-UHFFFAOYSA-N |
2,5-Dimethoxy-4-iodoamphetamine
2,5-Dimethoxy-4-iodoamphetamine (also known as 4-DOI, 4-Iodo-2,5-dimethoxyphenylisopropylamine, 2,5-Dimethoxy-4-iodophenylisopropylamine, 1-(2,5-Dimethoxy-4-iodophenyl)-2-aminopropane, 1-(4-Iodo-2,5-dimethoxyphenyl)-2-aminopropane, 4-Iodo-2,5-dimethoxyamphetamine, 2-(4-iodo-2,5-dimethoxyphenyl)-1-methylethylamine, DOI-P, (+/-)-1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane or Racemic DOI) is a hallucinogens substance of the 2,5-dimethoxyamphetamine class.
Chemistry
2,5-Dimethoxy-4-iodoamphetamine is typically found in the form of its hydrochloride salt.
Stereochemistry
(RS)-2,5-Dimethoxy-4-iodoamphetamine is a racemic mixture of the optical stereoisomers.See also
External links
- 2,5-Dimethoxy-4-iodoamphetamine (Wikipedia)
- 2,5-Dimethoxy-4-iodoamphetamine (Wikidata)
- 2,5-Dimethoxy-4-iodoamphetamine (PubChem)
- 2,5-Dimethoxy-4-iodoamphetamine (ChemSpider)
- 2,5-Dimethoxy-4-iodoamphetamine (ChEMBL)
- 2,5-Dimethoxy-4-iodoamphetamine (ChEBI)
- 2,5-Dimethoxy-4-iodoamphetamine (Common Chemistry)
- 2,5-Dimethoxy-4-iodoamphetamine (HMDB)
- 2,5-Dimethoxy-4-iodoamphetamine (UNII)
- 2,5-Dimethoxy-4-iodoamphetamine (EPA DSSTox)