Tris(4-tert-butylphenyl)sulfonium triflate - electronic grade, ≥99% metals basis , CAS No.134708-14-8

CAS: 134708-14-8 Cat. No.: T476344 Peso molecular: 580.76

GRADE & PURITY Electronic grade, ≥99% metals basis

Synonyms

Tris(4-(tert-butyl)phenyl)sulfonium trifluoromethanesulfonate | Tris(4-tert-butylphenyl)sulfonium triflate | Tris(4-tert-butylphenyl)sulfanium trifluoromethanesulfonate | Sulfonium, tris[(1,1-dimethylethyl)phenyl]-, 1,1,1-trifluoromethanesulfonate | tris(

Storage

Store at 2-8°C,Protected from light,Argon charged,Desiccated

Shipped In

Wet ice

Descripción general

Description

Cationic photoinitiator. Photoacid generator.

Specifications

Sinónimos

Tris(4-(tert-butyl)phenyl)sulfonium trifluoromethanesulfonate | Tris(4-tert-butylphenyl)sulfonium triflate | Tris(4-tert-butylphenyl)sulfanium trifluoromethanesulfonate | Sulfonium, tris[(1, 1-dimethylethyl)phenyl]-, 1, 1, 1-trifluoromethanesulfonate | tris(

Especificaciones y pureza

electronic grade, ≥99% metals basis

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Protected from light, Argon charged, Desiccated

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Grado

Electronic grade

Pureza

≥99% metals basis

Nombres e identificadores

• Sonrisas canónicas: CC(C)(C)C1=CC=C(C=C1)[S+](C2=CC=C(C=C2)C(C)(C)C)C3=CC=C(C=C3)C(C)(C)C.C(F)(F)(F)S(=O)(=O)[O-]
• IUPAC Name: trifluoromethanesulfonate;tris(4-tert-butylphenyl)sulfanium
• InChIKey: HHMQUQRJNPTPAJ-UHFFFAOYSA-M
• INCHI: 1S/C30H39S.CHF3O3S/c1-28(2,3)22-10-16-25(17-11-22)31(26-18-12-23(13-19-26)29(4,5)6)27-20-14-24(15-21-27)30(7,8)9;2-1(3,4)8(5,6)7/h10-21H,1-9H3;(H,5,6,7)/q+1;/p-1
• Isómeros SMILES: CC(C)(C)C1=CC=C(C=C1)[S+](C2=CC=C(C=C2)C(C)(C)C)C3=CC=C(C=C3)C(C)(C)C.C(F)(F)(F)S(=O)(=O)[O-]
• CAS alternativo: 220155-94-2
• Peso molecular: 580.76

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Phenylpropanes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Phenylpropanes
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylpropanes
• Alternative Parents: Organosulfur compounds Organic salts Hydrocarbon derivatives
• Molecular Framework: Not available
• Substituents: Phenylpropane - Hydrocarbon derivative - Organic salt - Organosulfur compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenylpropanes. These are organic compounds containing a phenylpropane moiety.
• 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

Propiedades químicas y físicas

• Solubilidad: PGMEA: <1%γ-butyrolactone: ~25%ethyl lactate: ~5%
• Sensibilidad: Moisture sensitive；Light sensitive
• Punto de inflamación (°F): Not applicable
• Punto de inflamación (°C): Not applicable
• Punto de fusión (°C): 250-253℃ (lit.)
• Peso molecular: 580.800 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 6
• Exact Mass: 580.229 Da
• Monoisotopic Mass: 580.229 Da
• Topological Polar Surface Area: 66.600 Ų
• Heavy Atom Count: 39
• Formal Charge: 0
• Complexity: 596.000
• 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

XLogP3