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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items [Bis(trifluoroacetoxy)iodo]pentafluorobenzene - ≥97% , CAS No.14353-88-9
Synonyms
T70282 | B1616 | DTXSID20347823 | [Bis(trifluoroacetoxy)iodo]pentafluorobenzene, 97% | [(2,3,4,5,6-pentafluorophenyl)-(2,2,2-trifluoroacetyl)oxy-lambda3-iodanyl] 2,2,2-trifluoroacetate | BS-43999 | SY050534 | (Bis(trifluoroacetoxy)iodo)pentafluorobenzene
Storage
Argon charged,Room temperature
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Argon charged,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.
Descripción general Product Application：
Reactant or reagent for:
Oxidation of organic iodides using oxone and trifluoroacetic acid
Base hydrolysis
Oxidative cross-coupling of arenes
Oxidation of phenolic compounds with organohypervalent iodine
Aziridination of alkenes
Oxidation of organic compounds
Oxidative fragmentation of α-amino acids or β-amino alcohols
Oxidative biaryl coupling of thiophenes
Specifications Sinónimos
T70282 | B1616 | DTXSID20347823 | [Bis(trifluoroacetoxy)iodo]pentafluorobenzene, 97% | [(2, 3, 4, 5, 6-pentafluorophenyl)-(2, 2, 2-trifluoroacetyl)oxy-lambda3-iodanyl] 2, 2, 2-trifluoroacetate | BS-43999 | SY050534 | (Bis(trifluoroacetoxy)iodo)pentafluorobenzene
Especificaciones y pureza
≥97%
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Nombres e identificadores Pubchem Sid 488190802 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488190802 Sonrisas canónicas C1(=C(C(=C(C(=C1F)F)I(OC(=O)C(F)(F)F)OC(=O)C(F)(F)F)F)F)F IUPAC Name [(2,3,4,5,6-pentafluorophenyl)-(2,2,2-trifluoroacetyl)oxy-λ3-iodanyl] 2,2,2-trifluoroacetate InChIKey OQWAXRPJEPTTSZ-UHFFFAOYSA-N INCHI 1S/C10F11IO4/c11-1-2(12)4(14)6(5(15)3(1)13)22(25-7(23)9(16,17)18)26-8(24)10(19,20)21 Isómeros SMILES C1(=C(C(=C(C(=C1F)F)I(OC(=O)C(F)(F)F)OC(=O)C(F)(F)F)F)F)F WGK Alemania 3 PubChem CID 626316 Peso molecular 519.99 Reaxy-Rn 2030069
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 Halobenzenes Intermediate Tree Nodes Not available Direct Parent Iodobenzenes Alternative Parents Fluorobenzenes Dicarboxylic acids and derivatives Aryl iodides Aryl fluorides Alpha-halocarboxylic acid derivatives Carboxylic acid salts Organoiodides Organofluorides Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl fluorides Molecular Framework Aromatic homomonocyclic compounds Substituents Fluorobenzene - Iodobenzene - Aryl fluoride - Aryl halide - Aryl iodide - Dicarboxylic acid or derivatives - Alpha-halocarboxylic acid or derivatives - Alpha-halocarboxylic acid derivative - Carboxylic acid salt - Carboxylic acid derivative - Organofluoride - Organohalogen compound - Organic oxide - Organic oxygen compound - Carbonyl group - Alkyl halide - Alkyl fluoride - Organoiodide - Organooxygen compound - Organic salt - Hydrocarbon derivative - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as iodobenzenes. These are aromatic compounds containing one or more iodine atoms attached to a benzene. 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 Solubilidad Soluble in Methanol Sensibilidad Light Sensitive,Air Sensitive Punto de fusión (°C) 120 °C Peso molecular 519.990 g/mol XLogP3 5.500 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 15 Rotatable Bond Count 5 Exact Mass 519.867 Da Monoisotopic Mass 519.867 Da Topological Polar Surface Area 52.600 Ų Heavy Atom Count 26 Formal Charge 0 Complexity 494.000 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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