Determine the necessary mass, volume, or concentration for preparing a solution.
≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice 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.
Zopiclone N-oxide (RP 29753) is a less active metabolite of Zopiclone. Zopiclone N-oxide is also an impurity of Eszopiclone and is formed by the oxidation of Eszopiclone.
| Sonrisas canónicas | C[N+]1(CCN(CC1)C(=O)OC2C3=NC=CN=C3C(=O)N2C4=NC=C(C=C4)Cl)[O-] |
|---|---|
| IUPAC Name | [6-(5-chloropyridin-2-yl)-5-oxo-7H-pyrrolo[3,4-b]pyrazin-7-yl] 4-methyl-4-oxidopiperazin-4-ium-1-carboxylate |
| InChIKey | IPTIKKTXLHVRKN-UHFFFAOYSA-N |
| INCHI | 1S/C17H17ClN6O4/c1-24(27)8-6-22(7-9-24)17(26)28-16-14-13(19-4-5-20-14)15(25)23(16)12-3-2-11(18)10-21-12/h2-5,10,16H,6-9H2,1H3 |
| Isómeros SMILES | C[N+]1(CCN(CC1)C(=O)OC2C3=NC=CN=C3C(=O)N2C4=NC=C(C=C4)Cl)[O-] |
| WGK Alemania | 1 |
| PubChem CID | 162548 |
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 |
| Clase | Pyrrolopyrazines |
| Subclass | Cyclopyrrolones |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Cyclopyrrolones |
| Alternative Parents | Piperazine carboxylic acids 2-heteroaryl carboxamides N-methylpiperazines Aryl chlorides Imidolactams Pyridines and derivatives Pyrazines Trialkyl amine oxides Carbamate esters Heteroaromatic compounds Tertiary carboxylic acid amides Lactams Organic carbonic acids and derivatives Trisubstituted amine oxides and derivatives Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides Organic zwitterions Organochlorides |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Cyclopyrrolone - Piperazine-1-carboxylic acid - 2-heteroaryl carboxamide - N-methylpiperazine - N-alkylpiperazine - Aryl chloride - Aryl halide - 1,4-diazinane - Piperazine - Pyrazine - Pyridine - Imidolactam - Trialkyl amine oxide - Carbamic acid ester - Tertiary carboxylic acid amide - Heteroaromatic compound - Carboxamide group - Lactam - Carbonic acid derivative - Trisubstituted n-oxide - Azacycle - Carboxylic acid derivative - N-oxide - Organopnictogen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organic oxide - Organic zwitterion - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Aromatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as cyclopyrrolones. These are compounds belonging to a family of pyridin-2-ylpyrrole based chemicals. The pyrrole is usually fused to a benzene, pyrimidine, or dithiin. |
| External Descriptors | Not available |
| Punto de inflamación (°F) | 48.2 °F |
|---|---|
| Punto de inflamación (°C) | 9 °C |