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224,000+ productos de investigación · Triple ISO certified · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items PD 168077 maleate - ≥97% , CAS No.630117-19-0
Synonyms
N-((4-(2-Cyanophenyl)-1-piperazinyl)methyl)-3-methylbenzamide (2Z)-2-butenedioate (1:1) | HY-21098A | N-(Methyl-4-(2-cyanophenyl)piperazinyl-3-methylbenzamide maleate | AKOS024256763 | PD168077 Maleate | PD-168077 maleate | PD 168,077 maleate | HMS3650G07
Storage
Store at -20°C,Desiccated
Shipped In
Ice chest + Ice pads
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Why this grade ≥97% 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
N-((4-(2-Cyanophenyl)-1-piperazinyl)methyl)-3-methylbenzamide (2Z)-2-butenedioate (1:1) | HY-21098A | N-(Methyl-4-(2-cyanophenyl)piperazinyl-3-methylbenzamide maleate | AKOS024256763 | PD168077 Maleate | PD-168077 maleate | PD 168, 077 maleate | HMS3650G07
Especificaciones y pureza
≥97%
Mecanismos bioquímicos y fisiológicos
A potent D4dopamine receptor agonist (Ki= 8.7 nM) with > 400-fold selectivity over D2and > 300-fold selectivity versus D3subtypes respectively. Induces synaptic translocation of CaMK II to postsynaptic sites in cultured prefrontal cortical neurons. Centra
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 488197809 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488197809 Sonrisas canónicas CC1=CC(=CC=C1)C(=O)NCN2CCN(CC2)C3=CC=CC=C3C#N.C(=CC(=O)O)C(=O)O IUPAC Name (Z)-but-2-enedioic acid;N-[[4-(2-cyanophenyl)piperazin-1-yl]methyl]-3-methylbenzamide InChIKey NAEUGRPISCANHO-BTJKTKAUSA-N INCHI 1S/C20H22N4O.C4H4O4/c1-16-5-4-7-17(13-16)20(25)22-15-23-9-11-24(12-10-23)19-8-3-2-6-18(19)14-21;5-3(6)1-2-4(7)8/h2-8,13H,9-12,15H2,1H3,(H,22,25);1-2H,(H,5,6)(H,7,8)/b;2-1- Isómeros SMILES CC1=CC(=CC=C1)C(=O)NCN2CCN(CC2)C3=CC=CC=C3C#N.C(=C\C(=O)O)\C(=O)O CAS alternativo 190383-31-4 Peso molecular 450.49
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 Phenylpiperazines Alternative Parents N-arylpiperazines m-Toluamides Benzamides Aniline and substituted anilines Benzonitriles Benzoyl derivatives Dialkylarylamines N-alkylpiperazines Unsaturated fatty acids Dicarboxylic acids and derivatives Secondary carboxylic acid amides Amino acids and derivatives Carboxylic acids Nitriles Azacyclic compounds Carbonyl compounds Organic oxides Hydrocarbon derivatives Molecular Framework Not available Substituents Phenylpiperazine - N-arylpiperazine - Benzamide - Benzoic acid or derivatives - M-toluamide - Toluamide - Benzonitrile - Benzoyl - Tertiary aliphatic/aromatic amine - Aniline or substituted anilines - Dialkylarylamine - Toluene - N-alkylpiperazine - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Fatty acyl - Unsaturated fatty acid - Fatty acid - Benzenoid - Tertiary amine - Carboxamide group - Amino acid or derivatives - Secondary carboxylic acid amide - Nitrile - Carbonitrile - Carboxylic acid - Carboxylic acid derivative - Azacycle - Organic nitrogen compound - Amine - Carbonyl group - Organic oxide - Cyanide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as phenylpiperazines. These are compounds containing a phenylpiperazine skeleton, which consists of a piperazine bound to a phenyl 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:DMSO, Max Conc. mg/mL: 45.05, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 11.26, Max Conc. mM: 25 Peso molecular 450.500 g/mol XLogP3 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 8 Rotatable Bond Count 6 Exact Mass 450.19 Da Monoisotopic Mass 450.19 Da Topological Polar Surface Area 134.000 Ų Heavy Atom Count 33 Formal Charge 0 Complexity 610.000 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 2
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