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≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
DOT1L inhibitors
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Classe | Quinolines and derivatives |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Quinolines and derivatives |
| Alternative Parents | Alkylarylthioethers Alkyl aryl ethers Pyridines and derivatives Benzenoids Triazoles Heteroaromatic compounds Primary carboxylic acid amides Sulfenyl compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Quinoline - Aryl thioether - Alkyl aryl ether - Alkylarylthioether - Pyridine - Benzenoid - Azole - Heteroaromatic compound - 1,2,4-triazole - Carboxamide group - Primary carboxylic acid amide - Carboxylic acid derivative - Ether - Azacycle - Thioether - Sulfenyl compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organopnictogen compound - Aromatic heteropolycyclic compound |
| Descrição | This compound belongs to the class of organic compounds known as quinolines and derivatives. These are compounds containing a quinoline moiety, which consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Item |
|---|---|---|---|
| Certificate of Analysis | Apr 08, 2026 | W418299 | |
| Certificate of Analysis | Mar 18, 2026 | W418299 | |
| Certificate of Analysis | Mar 18, 2026 | W418299 | |
| Certificate of Analysis | Mar 18, 2026 | W418299 | |
| Certificate of Analysis | Mar 18, 2026 | W418299 | |
| Certificate of Analysis | Mar 18, 2026 | W418299 | |
| Certificate of Analysis | Mar 18, 2026 | W418299 | |
| Certificate of Analysis | Mar 18, 2026 | W418299 | |
| Certificate of Analysis | Mar 18, 2026 | W418299 | |
| Certificate of Analysis | Mar 18, 2026 | W418299 | |
| Certificate of Analysis | Mar 18, 2026 | W418299 |
| DMSO (mM) Solubilidade máxima | 10 |
|---|---|
| Peso molecular | 329.400 g/mol |
| XLogP3 | 1.000 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 6 |
| Exact Mass | 329.095 Da |
| Monoisotopic Mass | 329.095 Da |
| Topological Polar Surface Area | 121.000 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 413.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| 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 |