2,4-DMA

Summary

2,4-DMA is a group of stereoisomers^[1]. 2,4-DMA draws 3 Wikipedia views per month (group_of_stereoisomers category, ranking #217 of 1,063).^[2]

Key Facts

• 2,4-DMA is credited with the discovery of Alexander Shulgin^[3].
• 2,4-DMA's instance of is recorded as group of stereoisomers^[4].
• 2,4-DMA's chemical structure is recorded as 2,4-DMA.svg^[5].
• 2,4-DMA's CAS Registry Number is recorded as 23690-13-3^[6].
• 2,4-DMA's canonical SMILES is recorded as CC(CC1=C(C=C(C=C1)OC)OC)N^[7].
• 2,4-DMA's InChI is recorded as InChI=1S/C11H17NO2/c1-8(12)6-9-4-5-10(13-2)7-11(9)14-3/h4-5,7-8H,6,12H2,1-3H3^[8].
• 2,4-DMA's InChIKey is recorded as DQWOZMUBHQPFFF-UHFFFAOYSA-N^[9].
• 2,4-DMA's chemical formula is recorded as C₁₁H₁₇NO₂^[10].
• 2,4-DMA's subclass of is recorded as dimethoxyamphetamines^[11].
• 2,4-DMA's Commons category is recorded as 2,4-Dimethoxyamphetamine^[12].
• 2,4-DMA's has part is recorded as carbon^[13].
• 2,4-DMA's has part is recorded as hydrogen^[14].
• 2,4-DMA's has part is recorded as nitrogen^[15].
• 2,4-DMA's has part is recorded as oxygen^[16].
• 2,4-DMA's ChEMBL ID is recorded as CHEMBL282734^[17].
• 2,4-DMA's UNII is recorded as GT33R7Q58G^[18].
• 2,4-DMA's ChemSpider ID is recorded as 124411^[19].
• 2,4-DMA's PubChem CID is recorded as 141047^[20].
• 2,4-DMA's described by source is recorded as Phenethylamines I Have Known And Loved^[21].
• 2,4-DMA's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+195.126'}^[22].
• 2,4-DMA's Nikkaji ID is recorded as J273.465F^[23].
• 2,4-DMA's subject has role is recorded as psychoactive drug^[24].
• 2,4-DMA's subject has role is recorded as stimulant^[25].
• 2,4-DMA's SureChEMBL ID is recorded as 266899^[26].
• 2,4-DMA's DSSTox substance ID is recorded as DTXSID90874252^[27].

Body

Works and Contributions

2,4-DMA is credited with the discovery of Alexander Shulgin^[3].

Why It Matters

2,4-DMA draws 3 Wikipedia views per month (group_of_stereoisomers category, ranking #217 of 1,063).^[2]