Methyl 4-Tolyl Sulfoxide - ≥98% , CAS No.934-72-5

CAS: 934-72-5 Cat. No.: M304998 Peso molecular: 154.23 Número EC: 890-047-0

GRADE & PURITY ≥98%

Synonyms

Benzene, 1-methyl-4-[(R)-methylsulfinyl]- | DTXSID401347144 | 1-Methyl-4-(methylsulphinyl)benzene | Methyl p-tolyl sulfoxide, 97% | Methyl 4-methylphenylsulfoxide | NSC141186 | NSC-141186 | SCHEMBL280535 | CCRIS 3423 | FT-0693563 | T73083 | 1-methyl-4-met

Storage

Store at 2-8°C,Argon charged,Desiccated

Shipped In

Wet ice

Descripción general

Product Describtion:

Methyl p-tolyl sulfoxide (MTSO), an alkyl-substituted p-tolyl sulfoxide, is a Lewis base. It behaves as an activator of silicon tetrachloride that is employed in aza-Diels-Alder reaction.

Product Application:

Methyl p-tolyl sulfoxide may be used as a catalyst in the preparation of homoallylic alcohols by the allylation of aldehydes with allyltrichlorosilane. It may be used as a ligand in the synthesis of molybdenum chlorocomplexes.

Specifications

Sinónimos

Benzene, 1-methyl-4-[(R)-methylsulfinyl]- | DTXSID401347144 | 1-Methyl-4-(methylsulphinyl)benzene | Methyl p-tolyl sulfoxide, 97% | Methyl 4-methylphenylsulfoxide | NSC141186 | NSC-141186 | SCHEMBL280535 | CCRIS 3423 | FT-0693563 | T73083 | 1-methyl-4-met

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, 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.

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504757089
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504757089
• Sonrisas canónicas: CC1=CC=C(C=C1)S(=O)C
• IUPAC Name: 1-methyl-4-methylsulfinylbenzene
• InChIKey: FEVALTJSQBFLEU-UHFFFAOYSA-N
• INCHI: 1S/C8H10OS/c1-7-3-5-8(6-4-7)10(2)9/h3-6H,1-2H3
• Isómeros SMILES: CC1=CC=C(C=C1)S(=O)C
• Peso molecular: 154.23
• Reaxy-Rn: 1906006
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1906006&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Phenyl sulfoxides
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenyl sulfoxides
• Alternative Parents: Toluenes Sulfoxides Sulfinyl compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenyl sulfoxide - Toluene - Sulfoxide - Sulfinyl compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenyl sulfoxides. These are organosulfur compounds containing a sulfoxide group substituted with a phenyl 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

Propiedades químicas y físicas

• Solubilidad: Soluble in Methanol
• Sensibilidad: Moisture sensitive.
• Punto de ebullición (°C): 114°C/2mmHg(lit.)
• Punto de fusión (°C): 42 °C
• Peso molecular: 154.230 g/mol
• XLogP3: 1.400
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 154.045 Da
• Monoisotopic Mass: 154.045 Da
• Topological Polar Surface Area: 36.300 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 125.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Linhao Wang, Jia Wei, Jiangkai Huo, Wei Ji, Xiaohui Zhang, Yanan Li, Jiamei Li, Nan Cui, Wenhao Yan, Yuxin Zhao, Jun Li, Ju Wang.  (2025)  Harnessing Electronically Core-Shell CoFe Alloy-Carbon from Prussian Blue Analogues for Efficient Pollutant Abatement via Peracetic Acid Activation: Dual Reactive Species Generation and Synergistic Mechanisms.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2025.125284]