10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -80°C Ships Dry ice packs + Cold packs 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.
promoting myelination (treat human neurodegenerative diseases); protect oligodendrocyte viability and differentiation under inflammatory conditions; improving the efficacy of viral transduction of cells; Inhibitors of 7-Dehydrocholesterol Reductase; promoting remyelination; promoting myelination; promote remyelination; inhibitors of JARID1A and JARID1B; modulating Prostaglandin signaling; hOCT1 and hOCT2 substrates ; improved viral transduction; vesicular acetylcholine transporter inhibitors; Inhibition of Cholinergic Signaling; vesicular acetylcholine transporter inhibitors; altering the lifespan of a eukaryotic organism; antidepressant; inhibit transport-P in peptidergic neurons; protein kinase C activation; α-Adrenoceptor blocking properties; acetylcholine transport blocker;
| Pubchem Sid | 528767723 |
|---|---|
| Sonrisas canónicas | C1CN(CCN1C2=NC=CC=N2)C(=O)C=CC3=CC=CC=C3 |
| IUPAC Name | (E)-3-phenyl-1-(4-pyrimidin-2-ylpiperazin-1-yl)prop-2-en-1-one |
| InChIKey | XCGMDDSRZZXNOE-BQYQJAHWSA-N |
| INCHI | 1S/C17H18N4O/c22-16(8-7-15-5-2-1-3-6-15)20-11-13-21(14-12-20)17-18-9-4-10-19-17/h1-10H,11-14H2/b8-7+ |
| Isómeros SMILES | C1CN(CCN1C2=NC=CC=N2)C(=O)/C=C/C3=CC=CC=C3 |
| PubChem CID | 6242130 |
| Peso molecular | 294.36 |
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 | Diazinanes |
| Subclass | Piperazines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | N-arylpiperazines |
| Alternative Parents | Cinnamic acids and derivatives Styrenes Dialkylarylamines Aminopyrimidines and derivatives Tertiary carboxylic acid amides Heteroaromatic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Cinnamic acid or derivatives - N-arylpiperazine - Styrene - Dialkylarylamine - Aminopyrimidine - Monocyclic benzene moiety - Pyrimidine - Benzenoid - Heteroaromatic compound - Tertiary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Azacycle - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Amine - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as n-arylpiperazines. These are organic compounds containing a piperazine ring where the nitrogen ring atom carries an aryl group. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 G2411012 | Certificate of Analysis | May 13, 2026 | W421325 |
| Peso molecular | 294.350 g/mol |
|---|---|
| XLogP3 | 2.000 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 3 |
| Exact Mass | 294.148 Da |
| Monoisotopic Mass | 294.148 Da |
| Topological Polar Surface Area | 49.300 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 378.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 1 |
