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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Ro 04-6790 - Moligand™, ≥98%(HPLC) , Antagonist of 5-HT 6 receptor, CAS No.202466-68-0, Antagonist of 5-HT 6 receptor
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%(HPLC) Synonyms
Kiton Black HA | Q855636 | L000511 | 4-Amino-N-(2,6-bis-dimethylamino-pyrimidin-4-yl)-benzenesulfonamide | CU78RAR5ZH | DTXSID50187476 | Ro 04-6790 dihydrochloride | (4-amino-N-[2,6-bis(methylamino)-4-pyrimidinyl]-benzenesulfonamide) | 4-Azanyl-N-(2,6-bis
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™, ≥98%(HPLC) Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C 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
Kiton Black HA | Q855636 | L000511 | 4-Amino-N-(2, 6-bis-dimethylamino-pyrimidin-4-yl)-benzenesulfonamide | CU78RAR5ZH | DTXSID50187476 | Ro 04-6790 dihydrochloride | (4-amino-N-[2, 6-bis(methylamino)-4-pyrimidinyl]-benzenesulfonamide) | 4-Azanyl-N-(2, 6-bis
Especificaciones y pureza
Moligand™, ≥98%(HPLC)
Mecanismos bioquímicos y fisiológicos
Potent and selective 5-HT6receptor antagonist (pKivalues are 7.26 and 7.35 at rat and human 5-HT6receptors respectively). Displays no affinity at a range of other receptors (IC50> 10μM). Induces stretching behavior in ratsin vivo.
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Mecanismo de acción
Antagonist of 5-HT 6 receptor
Nombres e identificadores Sonrisas canónicas CNC1=CC(=NC(=N1)NC)NS(=O)(=O)C2=CC=C(C=C2)N IUPAC Name 4-amino-N-[2,6-bis(methylamino)pyrimidin-4-yl]benzenesulfonamide InChIKey JELFWSXQTXRMAJ-UHFFFAOYSA-N INCHI 1S/C12H16N6O2S/c1-14-10-7-11(17-12(15-2)16-10)18-21(19,20)9-5-3-8(13)4-6-9/h3-7H,13H2,1-2H3,(H3,14,15,16,17,18) Isómeros SMILES CNC1=CC(=NC(=N1)NC)NS(=O)(=O)C2=CC=C(C=C2)N WGK Alemania 3 RTECS DA9462500 CAS alternativo 202466-68-0 PubChem CID 5312145 Términos de entrada MeSH 4-amino-N-(2,6 bis-methylamino-pyrimidin-4-yl)-benzene sulfonamide;Ro 04-6790;Ro 4-6790;Ro4-6790 Peso molecular 308.36
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 Benzenoids Clase Benzene and substituted derivatives Subclass Benzenesulfonamides Intermediate Tree Nodes Not available Direct Parent Aminobenzenesulfonamides Alternative Parents Benzenesulfonyl compounds Aniline and substituted anilines Secondary alkylarylamines Aminopyrimidines and derivatives Organosulfonamides Imidolactams Heteroaromatic compounds Aminosulfonyl compounds Azacyclic compounds Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents Aminobenzenesulfonamide - Benzenesulfonyl group - Aniline or substituted anilines - Aminopyrimidine - Secondary aliphatic/aromatic amine - Pyrimidine - Organosulfonic acid amide - Imidolactam - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Heteroaromatic compound - Secondary amine - Organoheterocyclic compound - Azacycle - Hydrocarbon derivative - Organic nitrogen compound - Amine - Organic oxide - Organopnictogen compound - Primary amine - Organosulfur compound - Organic oxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as aminobenzenesulfonamides. These are organic compounds containing a benzenesulfonamide moiety with an amine group attached to the benzene ring. 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: 30.84, Max Conc. mM: 100 Peso molecular 308.360 g/mol XLogP3 1.700 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 8 Rotatable Bond Count 5 Exact Mass 308.106 Da Monoisotopic Mass 308.106 Da Topological Polar Surface Area 130.000 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 418.000 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 1
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