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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items CP 809101 hydrochloride - ≥98% , CAS No.1215721-40-6
Synonyms
HY-15543A | 2-[(3-chlorophenyl)methoxy]-6-piperazin-1-ylpyrazine;hydrochloride | NMUNRTCTDLORDR-UHFFFAOYSA-N | 2-[(3-chlorophenyl)methoxy]-6-(piperazin-1-yl)pyrazine hydrochloride | 2-[(3-CHLOROPHENYL)METHOXY]-6-(1-PIPERAZINYL)PYRAZINE HYDROCHLORIDE | 2-[
Storage
Store at -20°C,Desiccated
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C,Desiccated Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
HY-15543A | 2-[(3-chlorophenyl)methoxy]-6-piperazin-1-ylpyrazine;hydrochloride | NMUNRTCTDLORDR-UHFFFAOYSA-N | 2-[(3-chlorophenyl)methoxy]-6-(piperazin-1-yl)pyrazine hydrochloride | 2-[(3-CHLOROPHENYL)METHOXY]-6-(1-PIPERAZINYL)PYRAZINE HYDROCHLORIDE | 2-[
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Potent and selective 5-HT2C receptor agonist (pEC50 values for human 5-HT2C, 5-HT2B and 5-HT2A receptors are 9.96, 7.19 and 6.81, respectively). Inhibits state avoidance response (CAR) in rats after subcutaneous administration and inhibits PCP and amphe
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Desiccated
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Pubchem Sid 504771522 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504771522 Sonrisas canónicas C1CN(CCN1)C2=CN=CC(=N2)OCC3=CC(=CC=C3)Cl.Cl IUPAC Name 2-[(3-chlorophenyl)methoxy]-6-piperazin-1-ylpyrazine;hydrochloride InChIKey NMUNRTCTDLORDR-UHFFFAOYSA-N INCHI 1S/C15H17ClN4O.ClH/c16-13-3-1-2-12(8-13)11-21-15-10-18-9-14(19-15)20-6-4-17-5-7-20;/h1-3,8-10,17H,4-7,11H2;1H Isómeros SMILES C1CN(CCN1)C2=CN=CC(=N2)OCC3=CC(=CC=C3)Cl.Cl PubChem CID 56972220 Peso molecular 341.2
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Clase Diazinanes Subclass Piperazines Intermediate Tree Nodes Not available Direct Parent N-arylpiperazines Alternative Parents Dialkylarylamines Chlorobenzenes Aminopyrazines Alkyl aryl ethers Imidolactams Aryl chlorides Heteroaromatic compounds Dialkylamines Azacyclic compounds Organochlorides Hydrochlorides Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents N-arylpiperazine - Dialkylarylamine - Alkyl aryl ether - Aminopyrazine - Chlorobenzene - Halobenzene - Imidolactam - Benzenoid - Aryl chloride - Aryl halide - Pyrazine - Monocyclic benzene moiety - Heteroaromatic compound - Tertiary amine - Azacycle - Secondary amine - Secondary aliphatic amine - Ether - Hydrochloride - Hydrocarbon derivative - Amine - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Organohalogen compound - Organochloride - Organonitrogen 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 Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Solvent:water, Max Conc. mg/mL: 6.82, Max Conc. mM: 20; Solvent:DMSO, Max Conc. mg/mL: 34.12, Max Conc. mM: 100 Peso molecular 341.200 g/mol XLogP3 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 4 Exact Mass 340.086 Da Monoisotopic Mass 340.086 Da Topological Polar Surface Area 50.300 Ų Heavy Atom Count 22 Formal Charge 0 Complexity 314.000 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 2
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