Determine the necessary mass, volume, or concentration for preparing a solution.
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Check lot-specific COA for exact specifications.
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.
| Sorrisi canonici | N#Cc1cc(cnc1N1CCN(CC1)c1noc(n1)C(C)C)c1ccc(c(c1)F)n1cnn(c1=O)[C@@H]1COCC1 |
|---|---|
| IUPAC Name | 5-[3-fluoro-4-[5-oxo-1-[(3S)-oxolan-3-yl]-1,2,4-triazol-4-yl]phenyl]-2-[4-(5-propan-2-yl-1,2,4-oxadiazol-3-yl)piperazin-1-yl]pyridine-3-carbonitrile |
| InChIKey | READJNFYOAOOFN-NRFANRHFSA-N |
| INCHI | 1S/C27H28FN9O3/c1-17(2)25-32-26(33-40-25)35-8-6-34(7-9-35)24-19(13-29)11-20(14-30-24)18-3-4-23(22(28)12-18)36-16-31-37(27(36)38)21-5-10-39-15-21/h3-4,11-12,14,16-17,21H,5-10,15H2,1-2H3/t21-/m0/s1 |
| Isomeri SMILES | CC(C)C1=NC(=NO1)N2CCN(CC2)C3=C(C=C(C=N3)C4=CC(=C(C=C4)N5C=NN(C5=O)[C@H]6CCOC6)F)C#N |
| PubChem CID | 86281591 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Classe | Diazinanes |
| Subclass | Piperazines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Pyridinylpiperazines |
| Alternative Parents | Phenylpyridines N-arylpiperazines Phenyl-1,2,4-triazoles 3-pyridinecarbonitriles Dialkylarylamines Aminopyridines and derivatives Fluorobenzenes Imidolactams Aryl fluorides Oxolanes 1,2,4-oxadiazoles Heteroaromatic compounds Oxacyclic compounds Nitriles Dialkyl ethers Azacyclic compounds Hydrocarbon derivatives Organic oxides Organofluorides |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | 3-phenylpyridine - Pyridinylpiperazine - N-arylpiperazine - Phenyltriazole - Phenyl-1,2,4-triazole - Dialkylarylamine - 3-pyridinecarbonitrile - Aminopyridine - Fluorobenzene - Halobenzene - Imidolactam - Benzenoid - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Pyridine - Heteroaromatic compound - 1,2,4-oxadiazole - Azole - 1,2,4-triazole - Triazole - Oxolane - Oxadiazole - Azacycle - Oxacycle - Dialkyl ether - Ether - Carbonitrile - Nitrile - Organic nitrogen compound - Amine - Organic oxygen compound - Cyanide - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organohalogen compound - Organofluoride - Organonitrogen compound - Aromatic heteromonocyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as pyridinylpiperazines. These are compounds containing a pyridinylpiperazine skeleton, which consists of a pyridine linked (not fused) to a piperazine by a bond by a single bond that is not part of a ring. |
| External Descriptors | Not available |
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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