Hexyl p-Toluenesulfonate - ≥98%(GC) , CAS No.3839-35-8

CAS: 3839-35-8 Cat. No.: H157121 Peso molecular: 256.36 Número EC: 112-719-8

GRADE & PURITY ≥98%(GC)

Synonyms

InChI=1/C13H20O3S/c1-3-4-5-6-11-16-17(14,15)13-9-7-12(2)8-10-13/h7-10H,3-6,11H2,1-2H | hexyl tosylate | MFCD00059439 | benzenesulfonic acid, 4-methyl-, hexyl ester | p-Toluenesulfonic acid n-hexyl ester | SY054269 | T0883 | EN300-7006895 | p-Toluenesulfon

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

InChI=1/C13H20O3S/c1-3-4-5-6-11-16-17(14, 15)13-9-7-12(2)8-10-13/h7-10H, 3-6, 11H2, 1-2H | hexyl tosylate | MFCD00059439 | benzenesulfonic acid, 4-methyl-, hexyl ester | p-Toluenesulfonic acid n-hexyl ester | SY054269 | T0883 | EN300-7006895 | p-Toluenesulfon

Especificaciones y pureza

≥98%(GC)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%(GC)

Nombres e identificadores

• Pubchem Sid: 504757892
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504757892
• Sonrisas canónicas: CCCCCCOS(=O)(=O)C1=CC=C(C=C1)C
• IUPAC Name: hexyl 4-methylbenzenesulfonate
• InChIKey: IVQOVYWBHRSGJI-UHFFFAOYSA-N
• INCHI: 1S/C13H20O3S/c1-3-4-5-6-11-16-17(14,15)13-9-7-12(2)8-10-13/h7-10H,3-6,11H2,1-2H3
• Isómeros SMILES: CCCCCCOS(=O)(=O)C1=CC=C(C=C1)C
• Peso molecular: 256.36
• Reaxy-Rn: 2697258
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2697258&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Benzenesulfonic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzenesulfonate esters
• Alternative Parents: p-Methylbenzenesulfonates Tosyl compounds Benzenesulfonyl compounds Arylsulfonic acids and derivatives Organosulfonic acid esters Sulfonyls Organooxygen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Benzenesulfonate ester - P-methylbenzenesulfonate - Tosyl compound - Arylsulfonic acid or derivatives - Benzenesulfonyl group - Toluene - Organosulfonic acid ester - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Organic oxide - Organosulfur compound - Organooxygen compound - Organic oxygen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as benzenesulfonate esters. These are arenesulfonate esters that result from the formal condensation of the hydroxy group of an alcohol, enol, phenol or heteroarenol with benzenesulfonic acid.
• 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

• Sensibilidad: Moisture Sensitive
• Punto de ebullición (°C): 197°C
• Peso molecular: 256.360 g/mol
• XLogP3: 3.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 7
• Exact Mass: 256.113 Da
• Monoisotopic Mass: 256.113 Da
• Topological Polar Surface Area: 51.800 Ų
• Heavy Atom Count: 17
• Formal Charge: 0
• Complexity: 284.000
• 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