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Synonyms
4-(Trifluoromethoxy)phenol | 4-(trifluoromethoxy)-phenol | p-Trifluoromethoxy phenol | 4-(Trifluoromethoxy)phenol, 98% | EINECS 212-583-0 | MLCUUJQEMZNLPZ-UHFFFAOYSA-N | 4-(trifluoromethyloxy)-phenol | DTXSID60232002 | Phenol, 4-(trifluoromethoxy)- | R-2-
Storage
Protected from light,Argon charged,Room temperature
Descripción general 4-(Trifluoromethoxy)phenol was employed in the catalytic enantioselective synthesis of esters.
Specifications Sinónimos
4-(Trifluoromethoxy)phenol | 4-(trifluoromethoxy)-phenol | p-Trifluoromethoxy phenol | 4-(Trifluoromethoxy)phenol, 98% | EINECS 212-583-0 | MLCUUJQEMZNLPZ-UHFFFAOYSA-N | 4-(trifluoromethyloxy)-phenol | DTXSID60232002 | Phenol, 4-(trifluoromethoxy)- | R-2-
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Protected from light, Argon charged, Room temperature
Nombres e identificadores Pubchem Sid 504754477 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504754477 Sonrisas canónicas C1=CC(=CC=C1O)OC(F)(F)F IUPAC Name 4-(trifluoromethoxy)phenol InChIKey WDRJNKMAZMEYOF-UHFFFAOYSA-N INCHI 1S/C7H5F3O2/c8-7(9,10)12-6-3-1-5(11)2-4-6/h1-4,11H Isómeros SMILES C1=CC(=CC=C1O)OC(F)(F)F WGK Alemania 2 PubChem CID 70015 Número ONU 2810 Peso molecular 178.11 Reaxy-Rn 1945934
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 Phenols Subclass 4-alkoxyphenols Intermediate Tree Nodes Not available Direct Parent 4-alkoxyphenols Alternative Parents Phenoxy compounds Phenol ethers 1-hydroxy-2-unsubstituted benzenoids Trihalomethanes Organooxygen compounds Organofluorides Hydrocarbon derivatives Alkyl fluorides Molecular Framework Aromatic homomonocyclic compounds Substituents 4-alkoxyphenol - Phenoxy compound - Phenol ether - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Trihalomethane - Organic oxygen compound - Halomethane - Hydrocarbon derivative - Organooxygen compound - Organofluoride - Organohalogen compound - Alkyl halide - Alkyl fluoride - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as 4-alkoxyphenols. These are phenols that carry an alkoxy group at the 4-position of 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 Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Sensibilidad Hygroscopic,light sensitive Índice de refracción 1.446-1.448 Punto de inflamación (°F) 186.8 °F Punto de inflamación (°C) 86℃ Punto de ebullición (°C) 80°C Punto de fusión (°C) 17-18°C Peso molecular 178.110 g/mol XLogP3 2.600 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 1 Exact Mass 178.024 Da Monoisotopic Mass 178.024 Da Topological Polar Surface Area 29.500 Ų Heavy Atom Count 12 Formal Charge 0 Complexity 138.000 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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