Polisulfonas - Mw ~80000 , CAS No.25135-51-7

CAS: 25135-51-7 Cat. No.: P303212 Fórmula: [C₆H₄-4-C(CH₃)₂C₆H₄-4-OC₆H₄-4-SO₂C₆H₄-4-O]n

CALIDAD & PUREZA Mw ~80000

Storage

Temperatura ambiente,Desecado

Shipped In

Normal

Especificaciones

Especificaciones y pureza

Mw ~80000

Condiciones de almacenamiento de almacenamiento

Temperatura ambiente,Desecado

Enviado en

Normal

Nombres e identificadores

Pubchem Sid

508816195

Sonrisas canónicas

CC(C)(C1=CC=C(C=C1)O)C2=CC=C(C=C2)O.C1=CC(=CC=C1O)S(=O)(=O)C2=CC=C(C=C2)O

IUPAC Name

4-[2-(4-hydroxyphenyl)propan-2-yl]phenol;4-(4-hydroxyphenyl)sulfonylphenol

InChIKey

ZUZZUJNBGCVPLQ-UHFFFAOYSA-N

INCHI

1S/C15H16O2.C12H10O4S/c1-15(2,11-3-7-13(16)8-4-11)12-5-9-14(17)10-6-12;13-9-1-5-11(6-2-9)17(15,16)12-7-3-10(14)4-8-12/h3-10,16-17H,1-2H3;1-8,13-14H

Isómeros SMILES

CC(C)(C1=CC=C(C=C1)O)C2=CC=C(C=C2)O.C1=CC(=CC=C1O)S(=O)(=O)C2=CC=C(C=C2)O

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Diphenylmethanes
• Intermediate Tree Nodes: Not available
• Direct Parent: Bisphenols
• Alternative Parents: Phenylpropanes Benzenesulfonyl compounds 1-hydroxy-2-unsubstituted benzenoids Sulfones Organooxygen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Not available
• Substituents: Bisphenol - Benzenesulfonyl group - Phenylpropane - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Sulfonyl - Sulfone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as bisphenols. These are methylenediphenols, HOC6H4CH2C6H4OH, commonly p,p-methylenediphenol, and their substitution products (generally derived from condensation of two equivalent amounts of a phenol with an aldehyde or ketone).
• 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

• Índice de refracción: 1.633