Triphenylsulfonium chloride - ≥98% , CAS No.4270-70-6

CAS: 4270-70-6 Cat. No.: T341870 Molecular Weight: 298.84 Beilstein Registry Number: 3920448 EC Number: 224-259-6 PubChem CID: 61343

GRADE & PURITY ≥98%

Synonyms

Triphenyl sulfide | J-002227 | Triphenylsulfoniumchloride | SY298159 | ZFEAYIKULRXTAR-UHFFFAOYSA-M | triphenylsulfanium;chloride | EINECS 224-259-6 | AKOS005258038 | SCHEMBL60006 | Sulfonium, triphenyl-, chloride | FT-0653962 | TRIPHENYLSULFONIUM CHLORIDE

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Overview

Application:

Triphenylsulfonium chloride is used as a key intermediate that is widely used in the new electronic chemicals such as semiconductor, LCD and TFT.

Specifications

Synonyms

Triphenyl sulfide | J-002227 | Triphenylsulfoniumchloride | SY298159 | ZFEAYIKULRXTAR-UHFFFAOYSA-M | triphenylsulfanium;chloride | EINECS 224-259-6 | AKOS005258038 | SCHEMBL60006 | Sulfonium, triphenyl-, chloride | FT-0653962 | TRIPHENYLSULFONIUM CHLORIDE

Specifications & Purity

≥98%

Storage

Protected from light, Room temperature, Argon charged

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488183483
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488183483
• Canonical Smiles: C1=CC=C(C=C1)[S+](C2=CC=CC=C2)C3=CC=CC=C3.[Cl-]
• IUPAC Name: triphenylsulfanium;chloride
• InChIKey: ZFEAYIKULRXTAR-UHFFFAOYSA-M
• INCHI: 1S/C18H15S.ClH/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;/h1-15H;1H/q+1;/p-1
• Isomeric SMILES: C1=CC=C(C=C1)[S+](C2=CC=CC=C2)C3=CC=CC=C3.[Cl-]
• WGK Germany: 3
• PubChem CID: 61343
• Molecular Weight: 298.84
• Beilstein: 3920448

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzene and substituted derivatives
• Alternative Parents: Organosulfur compounds Organic chloride salts Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Monocyclic benzene moiety - Hydrocarbon derivative - Organic chloride salt - Organic salt - Organosulfur compound - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of 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.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Soluble in water.
• Sensitivity: Light/Moisture sensitive
• Melt Point(°C): 298 °C
• Molecular Weight: 298.800 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 298.058 Da
• Monoisotopic Mass: 298.058 Da
• Topological Polar Surface Area: 1.000 Ų
• Heavy Atom Count: 20
• Formal Charge: 0
• Complexity: 202.000
• 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: 2

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