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224,000+ Forschungsprodukte · Triple ISO certified · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag auf Lager Clorsulon - ≥99% , CAS No.60200-06-8
Synonyms
BSPBio_000559 | CCG-213340 | Pharmakon1600-01505115 | Curatrem Drench, Curatrem Drench For Cattle | HMS3656F03 | SR-01000842150-2 | 4-amino-6-(1,2,2-trichlorovinyl)benzene-1,3-disulfonamide | Prestwick0_000540 | SPECTRUM1505115 | CAS-60200-06-8 | Clorsulo
Shipped In
Ice chest + Ice pads
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Why this grade ≥99% 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.
Übersicht Clorsulon is used in the treatment of Fasciola hepatica infections in calves and sheep.
Specifications Synonyme
BSPBio_000559 | CCG-213340 | Pharmakon1600-01505115 | Curatrem Drench, Curatrem Drench For Cattle | HMS3656F03 | SR-01000842150-2 | 4-amino-6-(1,2,2-trichlorovinyl)benzene-1,3-disulfonamide | Prestwick0_000540 | SPECTRUM1505115 | CAS-60200-06-8 | Clorsulo
Spezifikationen & Reinheit
≥99%
Biochemische und physiologische Mechanismen
A benzenedisulfonamide derivative with fasciolicidal activity. Anthelmintic (Trematodes).
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Namen und Kennungen Pubchem Sid 488183348 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488183348 Kanonisches Lächeln C1=C(C(=CC(=C1N)S(=O)(=O)N)S(=O)(=O)N)C(=C(Cl)Cl)Cl IUPAC Name 4-amino-6-(1,2,2-trichloroethenyl)benzene-1,3-disulfonamide InChIKey QOVTVIYTBRHADL-UHFFFAOYSA-N INCHI 1S/C8H8Cl3N3O4S2/c9-7(8(10)11)3-1-4(12)6(20(14,17)18)2-5(3)19(13,15)16/h1-2H,12H2,(H2,13,15,16)(H2,14,17,18) Isomere SMILES C1=C(C(=CC(=C1N)S(=O)(=O)N)S(=O)(=O)N)C(=C(Cl)Cl)Cl Molekulargewicht 380.66 Reaxy-Rn 2821757 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2821757&ln=
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 Klasse Benzene and substituted derivatives Subclass Benzenesulfonamides Intermediate Tree Nodes Not available Direct Parent Aminobenzenesulfonamides Alternative Parents Benzenesulfonyl compounds Aniline and substituted anilines Organosulfonamides Aminosulfonyl compounds Vinyl chlorides Chloroalkenes Primary amines Organopnictogen compounds Organochlorides Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Aminobenzenesulfonamide - Benzenesulfonyl group - Aniline or substituted anilines - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Chloroalkene - Haloalkene - Vinyl halide - Vinyl chloride - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Primary amine - Organosulfur compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organic nitrogen compound - Aromatic homomonocyclic compound Beschreibung 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.
3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Löslichkeit Soluble in Water Schmelzpunkt (°C) 194-203°C Molekulargewicht 380.700 g/mol XLogP3 1.200 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 3 Exact Mass 378.902 Da Monoisotopic Mass 378.902 Da Topological Polar Surface Area 163.000 Ų Heavy Atom Count 20 Formal Charge 0 Complexity 604.000 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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