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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 5-Chloro-3-iodopyridin-2-yl trifluoromethanesulfonate - ≥95% , CAS No.1261365-87-0
Synonyms
MFCD18374110 | 5-Chloro-3-iodopyridin-2-yltrifluoromethanesulfonate | 5-Chloro-3-iodopyridin-2-yl trifluoromethanesulfonate | Methanesulfonic acid, 1,1,1-trifluoro-, 5-chloro-3-iodo-2-pyridinyl ester | 1261365-87-0 | (5-chloro-3-iodopyridin-2-yl) trifluor
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Why this grade ≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal 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
MFCD18374110 | 5-Chloro-3-iodopyridin-2-yltrifluoromethanesulfonate | 5-Chloro-3-iodopyridin-2-yl trifluoromethanesulfonate | Methanesulfonic acid, 1, 1, 1-trifluoro-, 5-chloro-3-iodo-2-pyridinyl ester | 1261365-87-0 | (5-chloro-3-iodopyridin-2-yl) trifluor
Especificaciones y pureza
≥95%
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Sonrisas canónicas C1=C(C=NC(=C1I)OS(=O)(=O)C(F)(F)F)Cl IUPAC Name (5-chloro-3-iodopyridin-2-yl) trifluoromethanesulfonate InChIKey IRCLLYHKRRFPRN-UHFFFAOYSA-N INCHI 1S/C6H2ClF3INO3S/c7-3-1-4(11)5(12-2-3)15-16(13,14)6(8,9)10/h1-2H Isómeros SMILES C1=C(C=NC(=C1I)OS(=O)(=O)C(F)(F)F)Cl PubChem CID 50989401 Peso molecular 387.5
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 Organic acids and derivatives Clase Organic sulfonic acids and derivatives Subclass Organosulfonic acids and derivatives Intermediate Tree Nodes Alkanesulfonic acids and derivatives - Alkanesulfonic acids Direct Parent Trifluoromethanesulfonates Alternative Parents Polyhalopyridines 2-halopyridines Sulfonic acid esters Organosulfonic acid esters Sulfonyls Methanesulfonates Heteroaromatic compounds Trihalomethanes Vinyl iodides Vinyl chlorides Propargyl-type 1,3-dipolar organic compounds Iodoalkenes Chloroalkenes Azacyclic compounds Aldimines Organopnictogen compounds Organooxygen compounds Organoiodides Organofluorides Organochlorides Organic oxides Hydrocarbon derivatives Alkyl fluorides Molecular Framework Aromatic heteromonocyclic compounds Substituents Trifluoromethanesulfonate - Polyhalopyridine - 2-halopyridine - Organosulfonic acid ester - Sulfonic acid ester - Pyridine - Heteroaromatic compound - Sulfonyl - Methanesulfonate - Trihalomethane - Azacycle - Iodoalkene - Chloroalkene - Haloalkene - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Vinyl iodide - Vinyl halide - Vinyl chloride - Aldimine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Halomethane - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organoiodide - Organofluoride - Organochloride - Organohalogen compound - Imine - Alkyl halide - Alkyl fluoride - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as trifluoromethanesulfonates. These are alkanesulfonic acids, that contain a sulfonate group that is substituted with a trifluoromethyl 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 Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Peso molecular 387.500 g/mol XLogP3 3.200 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 2 Exact Mass 386.844 Da Monoisotopic Mass 386.844 Da Topological Polar Surface Area 64.599 Ų Heavy Atom Count 16 Formal Charge 0 Complexity 344.000 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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