3C-E

Summary

3C-E is a group of stereoisomers^[1]. 3C-E draws 19 Wikipedia views per month (group_of_stereoisomers category, ranking #207 of 1,063).^[2]

Key Facts

• 3C-E is credited with the discovery of Alexander Shulgin^[3].
• 3C-E's instance of is recorded as group of stereoisomers^[4].
• 3C-E's chemical structure is recorded as 3C-E.svg^[5].
• 3C-E's CAS Registry Number is recorded as 146849-92-5^[6].
• 3C-E's canonical SMILES is recorded as CCOc1c(cc(cc1OC)CC(C)N)OC^[7].
• 3C-E's InChI is recorded as InChI=1S/C13H21NO3/c1-5-17-13-11(15-3)7-10(6-9(2)14)8-12(13)16-4/h7-9H,5-6,14H2,1-4H3^[8].
• 3C-E's InChIKey is recorded as AHLXCGRWNKUNTQ-UHFFFAOYSA-N^[9].
• 3C-E's chemical formula is recorded as C₁₃H₂₁NO₃^[10].
• 3C-E's subclass of is recorded as phenethylamine^[11].
• 3C-E's has part is recorded as carbon^[12].
• 3C-E's has part is recorded as hydrogen^[13].
• 3C-E's has part is recorded as nitrogen^[14].
• 3C-E's has part is recorded as oxygen^[15].
• 3C-E's ChEMBL ID is recorded as CHEMBL128038^[16].
• 3C-E's Freebase ID is recorded as /m/04dlrw^[17].
• 3C-E's UNII is recorded as W9QX56V5RU^[18].
• 3C-E's ChemSpider ID is recorded as 21106237^[19].
• 3C-E's PubChem CID is recorded as 44350137^[20].
• 3C-E's described by source is recorded as Phenethylamines I Have Known And Loved^[21].
• 3C-E's mass is recorded as {'unit': 'Q483261', 'amount': '+239.152143532'}^[22].
• 3C-E's subject has role is recorded as psychoactive drug^[23].
• 3C-E's subject has role is recorded as psychedelic drug^[24].
• 3C-E's SureChEMBL ID is recorded as 5308245^[25].
• 3C-E's DSSTox substance ID is recorded as DTXSID40658382^[26].
• 3C-E's DSSTOX compound identifier is recorded as DTXCID80884042^[27].

Body

Works and Contributions

3C-E is credited with the discovery of Alexander Shulgin^[3].

Why It Matters

3C-E draws 19 Wikipedia views per month (group_of_stereoisomers category, ranking #207 of 1,063).^[2] 3C-E is known by 6 alternative names across languages and contexts.^[28]