DME

Summary

DME is a group of stereoisomers^[1]. DME draws 7 Wikipedia views per month (group_of_stereoisomers category, ranking #213 of 1,063).^[2]

Key Facts

• DME is credited with the discovery of Alexander Shulgin^[3].
• DME's instance of is recorded as group of stereoisomers^[4].
• DME's chemical structure is recorded as 3,4-Dimethoxy-β-hydroxyphenethylamine.svg^[5].
• DME's CAS Registry Number is recorded as 6924-15-8^[6].
• DME's canonical SMILES is recorded as COC1=C(C=C(C=C1)C(CN)O)OC^[7].
• DME's InChI is recorded as InChI=1S/C10H15NO3/c1-13-9-4-3-7(8(12)6-11)5-10(9)14-2/h3-5,8,12H,6,11H2,1-2H3^[8].
• DME's InChIKey is recorded as WIUFFBGZBFVVDL-UHFFFAOYSA-N^[9].
• DME's chemical formula is recorded as C₁₀H₁₅NO₃^[10].
• DME's subclass of is recorded as phenethylamine^[11].
• DME's has part is recorded as carbon^[12].
• DME's has part is recorded as hydrogen^[13].
• DME's has part is recorded as nitrogen^[14].
• DME's has part is recorded as oxygen^[15].
• DME's Freebase ID is recorded as /m/02q9z7k^[16].
• DME's UNII is recorded as F9TYB6AM4W^[17].
• DME's ChemSpider ID is recorded as 3088871^[18].
• DME's PubChem CID is recorded as 3863978^[19].
• DME's ChEBI ID is recorded as 125385^[20].
• DME's described by source is recorded as Phenethylamines I Have Known And Loved^[21].
• DME's mass is recorded as {'unit': 'Q483261', 'amount': '+197.105'}^[22].
• DME's Nikkaji ID is recorded as J532.144A^[23].
• DME's subject has role is recorded as psychoactive drug^[24].
• DME's SureChEMBL ID is recorded as 1966507^[25].
• DME's DSSTox substance ID is recorded as DTXSID50512380^[26].
• DME's DSSTOX compound identifier is recorded as DTXCID20972997^[27].

Body

Works and Contributions

DME is credited with the discovery of Alexander Shulgin^[3].

Why It Matters

DME draws 7 Wikipedia views per month (group_of_stereoisomers category, ranking #213 of 1,063).^[2] DME is known by 7 alternative names across languages and contexts.^[28]