Phenyl Trifluoromethanesulfonate - ≥98%(GC) , CAS No.17763-67-6

CAS: 17763-67-6 Cat. No.: P160509 Molecular Weight: 226.17 EC Number: 628-760-4 PubChem CID: 548641

GRADE & PURITY ≥98%(GC)

Synonyms

Phenyl trifluoromethanesulfonate | D92162 | AKOS025213101 | SCHEMBL780030 | FS-4226 | Trifluoromethanesulfonic Acid Phenyl Ester | trifluoro-methanesulfonic acid phenyl ester | Phenyl trifluoromethanesulfonate # | Methanesulfonic acid, trifluoro-, phenyl

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Synonyms

Phenyl trifluoromethanesulfonate | D92162 | AKOS025213101 | SCHEMBL780030 | FS-4226 | Trifluoromethanesulfonic Acid Phenyl Ester | trifluoro-methanesulfonic acid phenyl ester | Phenyl trifluoromethanesulfonate # | Methanesulfonic acid, trifluoro-, phenyl

Specifications & Purity

≥98%(GC)

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥98%(GC)

Names and Identifiers

• Pubchem Sid: 488190248
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488190248
• Canonical Smiles: C1=CC=C(C=C1)OS(=O)(=O)C(F)(F)F
• IUPAC Name: phenyl trifluoromethanesulfonate
• InChIKey: GRJHONXDTNBDTC-UHFFFAOYSA-N
• INCHI: 1S/C7H5F3O3S/c8-7(9,10)14(11,12)13-6-4-2-1-3-5-6/h1-5H
• Isomeric SMILES: C1=CC=C(C=C1)OS(=O)(=O)C(F)(F)F
• WGK Germany: 3
• PubChem CID: 548641
• Molecular Weight: 226.17
• Reaxy-Rn: 2052455

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Benzene and substituted derivatives
      • Subclass Phenoxy compounds

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Phenoxy compounds
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenoxy compounds
• Alternative Parents: Trifluoromethanesulfonates Sulfonic acid esters Organosulfonic acid esters Sulfonyls Methanesulfonates Trihalomethanes Organooxygen compounds Organofluorides Organic oxides Hydrocarbon derivatives Alkyl fluorides
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenoxy compound - Trifluoromethanesulfonate - Sulfonic acid ester - Organosulfonic acid ester - Methanesulfonate - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Trihalomethane - Halomethane - Alkyl fluoride - Organic oxide - Organosulfur compound - Organooxygen compound - Organofluoride - Organohalogen compound - Organic oxygen compound - Alkyl halide - Hydrocarbon derivative - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as phenoxy compounds. These are aromatic compounds contaning a phenoxy 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.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Moisture sensitive
• Refractive Index: 1.43
• Flash Point(°F): 159.8 °F
• Flash Point(°C): 71°C(lit.)
• Boil Point(°C): 62°C/13mmHg(lit.)
• Molecular Weight: 226.170 g/mol
• XLogP3: 2.500
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 225.991 Da
• Monoisotopic Mass: 225.991 Da
• Topological Polar Surface Area: 51.800 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 272.000
• 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

References

1. Siqi Sun, Pei Jia, Qizhang Huang, Min Lu, Po Lu, Feisong Qin, Guang Sun, Yanbo Gao, Xue Bai, Zhennan Wu, Yu Zhang.  (2022)  Spectrally stable and efficient pure-blue light-emitting diodes based on CsPb(Br/Cl)3 nanocrystals with surface passivation by organic sulfonate.  Materials Today Physics,      [PMID:] [10.1016/j.mtphys.2022.100899]