Tetrahidro-2H-piran-4-il p-tosilato - ≥98% , CAS No.97986-34-0

CAS: 97986-34-0 Cat. No.: T188922 Peso molecular: 256.3 PubChem CID: 13961807

GRADE & PURITY ≥98%

Synonyms

Tetrahydro-2H-pyran-4-yl p-tosylate | tetrahydropyran-4-yl 4-methylbenzenesulfonate | SCHEMBL435571 | EN300-132042 | 4-(4-methylphenylsulfonyloxy)tetrahydropyran | toluene-4-sulfonic acid tetrahydro-pyran-4-yl ester | toluene-4-sulfonic acid tetrahydropyr

Storage

Temperatura ambiente

Shipped In

Normal

Specifications

Sinónimos

Tetrahydro-2H-pyran-4-yl p-tosylate | tetrahydropyran-4-yl 4-methylbenzenesulfonate | SCHEMBL435571 | EN300-132042 | 4-(4-methylphenylsulfonyloxy)tetrahydropyran | toluene-4-sulfonic acid tetrahydro-pyran-4-yl ester | toluene-4-sulfonic acid tetrahydropyr

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Temperatura ambiente

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488198559
• Sonrisas canónicas: CC1=CC=C(C=C1)S(=O)(=O)OC2CCOCC2
• IUPAC Name: oxan-4-yl 4-methylbenzenesulfonate
• InChIKey: ZEERHWXRRLRIQO-UHFFFAOYSA-N
• INCHI: 1S/C12H16O4S/c1-10-2-4-12(5-3-10)17(13,14)16-11-6-8-15-9-7-11/h2-5,11H,6-9H2,1H3
• Isómeros SMILES: CC1=CC=C(C=C1)S(=O)(=O)OC2CCOCC2
• PubChem CID: 13961807
• Peso molecular: 256.3

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 Oxanes Organosulfonic acid esters Sulfonyls Oxacyclic compounds Dialkyl ethers Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Benzenesulfonate ester - P-methylbenzenesulfonate - Tosyl compound - Arylsulfonic acid or derivatives - Benzenesulfonyl group - Toluene - Oxane - Organosulfonic acid ester - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Dialkyl ether - Ether - Oxacycle - Organoheterocyclic compound - Organosulfur compound - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Aromatic heteromonocyclic 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

• Peso molecular: 256.320 g/mol
• XLogP3: 2.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 256.077 Da
• Monoisotopic Mass: 256.077 Da
• Topological Polar Surface Area: 61.000 Ų
• Heavy Atom Count: 17
• Formal Charge: 0
• Complexity: 319.000
• 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