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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Cyhalofop-butyl - analytical standard , CAS No.122008-85-9
Disponível para encomenda
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. Synonyms
(2R)-2-(4-(4-Cyano-2-fluorophenoxy)phenoxy)propanoic acid butyl ester | (R)-Butyl 2-(4-(4-cyano-2-fluorophenoxy)phenoxy)propanoate | CAS-122008-85-9 | HY-B0861 | NCGC00017168-02 | N-Ethyl-N-methyl-4,4-di(2-thienyl)-3-buten-2-amine | CCRIS 9267 | Cyhalofop
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Why this grade analytical standard Analytical standard 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 8 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
(2R)-2-(4-(4-Cyano-2-fluorophenoxy)phenoxy)propanoic acid butyl ester | (R)-Butyl 2-(4-(4-cyano-2-fluorophenoxy)phenoxy)propanoate | CAS-122008-85-9 | HY-B0861 | NCGC00017168-02 | N-Ethyl-N-methyl-4,4-di(2-thienyl)-3-buten-2-amine | CCRIS 9267 | Cyhalofop
Especificações e pureza
analytical standard
Condições de armazenamento de armazenamento
Room temperature
Nomes e identificadores Sorrisos canónicos
CCCCOC(=O)C(C)OC1=CC=C(C=C1)OC2=C(C=C(C=C2)C#N)F
IUPAC Name
butyl (2R)-2-[4-(4-cyano-2-fluorophenoxy)phenoxy]propanoate
InChIKey
TYIYMOAHACZAMQ-CQSZACIVSA-N
INCHI
1S/C20H20FNO4/c1-3-4-11-24-20(23)14(2)25-16-6-8-17(9-7-16)26-19-10-5-15(13-22)12-18(19)21/h5-10,12,14H,3-4,11H2,1-2H3/t14-/m1/s1
SMILES isoméricas
CCCCOC(=O)[C@@H](C)OC1=CC=C(C=C1)OC2=C(C=C(C=C2)C#N)F
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=13647697&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 Classe Benzene and substituted derivatives Subclass Diphenylethers Intermediate Tree Nodes Not available Direct Parent Diphenylethers Alternative Parents 2-phenoxypropionic acid esters Phenoxyacetic acid derivatives Diarylethers Phenoxy compounds Phenol ethers Benzonitriles Alkyl aryl ethers Fluorobenzenes Aryl fluorides Carboxylic acid esters Nitriles Monocarboxylic acids and derivatives Carbonyl compounds Hydrocarbon derivatives Organic oxides Organofluorides Organopnictogen compounds Molecular Framework Aromatic homomonocyclic compounds Substituents 2-phenoxypropionic acid ester - Diphenylether - Phenoxyacetate - Diaryl ether - Phenoxy compound - Benzonitrile - Phenol ether - Alkyl aryl ether - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Carboxylic acid ester - Carboxylic acid derivative - Ether - Monocarboxylic acid or derivatives - Carbonitrile - Nitrile - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organofluoride - Organic oxygen compound - Organopnictogen compound - Organic oxide - Organohalogen compound - Aromatic homomonocyclic compound Descrição This compound belongs to the class of organic compounds known as diphenylethers. These are aromatic compounds containing two benzene rings linked to each other through an ether group. External Descriptors Phenoxy herbicides 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.
Estrutura 3D Alvos associados (humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Ponto de inflamação (°F) 251.6°F Ponto de inflamação (°C) 122°C Ponto de fusão (°C) 49 °C Peso molecular 357.400 g/mol XLogP3 4.800 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 9 Exact Mass 357.138 Da Monoisotopic Mass 357.138 Da Topological Polar Surface Area 68.600 Ų Heavy Atom Count 26 Formal Charge 0 Complexity 483.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 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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