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≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Sonrisas canónicas | CCC(C1=NN=C(O1)NCC2=CC3=C(C=C2)C(=CC(=O)O3)C4=CC=C(C=C4)F)(C(F)(F)F)O |
|---|---|
| IUPAC Name | 4-(4-fluorophenyl)-7-[[[5-[(2S)-1,1,1-trifluoro-2-hydroxybutan-2-yl]-1,3,4-oxadiazol-2-yl]amino]methyl]chromen-2-one |
| InChIKey | MAOIDRRXRLYJNV-NRFANRHFSA-N |
| INCHI | 1S/C22H17F4N3O4/c1-2-21(31,22(24,25)26)19-28-29-20(33-19)27-11-12-3-8-15-16(10-18(30)32-17(15)9-12)13-4-6-14(23)7-5-13/h3-10,31H,2,11H2,1H3,(H,27,29)/t21-/m0/s1 |
| Isómeros SMILES | CC[C@](C1=NN=C(O1)NCC2=CC3=C(C=C2)C(=CC(=O)O3)C4=CC=C(C=C4)F)(C(F)(F)F)O |
| CAS alternativo | 910656-27-8 |
| PubChem CID | 11856170 |
| Términos de entrada MeSH | 4-(4-fluorophenyl)-7-(((5-(1-hydroxy-1-(trifluoromethyl)propyl)-1,3,4-oxadiazol-2-yl)amino)methyl)-2H-1-benzopyran-2-one;setileuton |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Phenylpropanoids and polyketides |
| Clase | Neoflavonoids |
| Subclass | Neoflavones |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Neoflavones |
| Alternative Parents | Coumarins and derivatives 1-benzopyrans Pyranones and derivatives Fluorobenzenes Aryl fluorides Tertiary alcohols 1,3,4-oxadiazoles Heteroaromatic compounds Lactones Fluorohydrins Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Aromatic alcohols Amines Alkyl fluorides Organic oxides Organofluorides |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | 4-phenylcoumarin - Coumarin - Benzopyran - 1-benzopyran - Fluorobenzene - Halobenzene - Pyranone - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Pyran - Benzenoid - Oxadiazole - Tertiary alcohol - 1,3,4-oxadiazole - Azole - Heteroaromatic compound - Lactone - Halohydrin - Fluorohydrin - Organoheterocyclic compound - Oxacycle - Azacycle - Alkyl halide - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Alkyl fluoride - Organohalogen compound - Alcohol - Organofluoride - Organonitrogen compound - Aromatic alcohol - Organooxygen compound - Amine - Aromatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as neoflavones. These are neoflavonoids with a structure based on the 4-phenylcoumarin skeleton. |
| External Descriptors | Not available |
| Peso molecular | 463.400 g/mol |
|---|---|
| XLogP3 | 3.800 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 6 |
| Exact Mass | 463.116 Da |
| Monoisotopic Mass | 463.116 Da |
| Topological Polar Surface Area | 97.500 Ų |
| Heavy Atom Count | 33 |
| Formal Charge | 0 |
| Complexity | 744.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |