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CAS 101691-65-0

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(Tetrahydro-2H-pyran-4-yl)methyl 4-methylbenzenesulphonate

Description:
(Tetrahydro-2H-pyran-4-yl)methyl 4-methylbenzenesulphonate, with CAS number 101691-65-0, is an organic compound characterized by its sulfonate ester functional group. This compound features a tetrahydro-2H-pyran ring, which contributes to its cyclic structure and potential reactivity. The presence of the 4-methylbenzenesulfonate moiety indicates that it has a hydrophobic aromatic component, which can influence its solubility and interaction with other substances. Generally, sulfonate esters are known for their stability and ability to act as good leaving groups in nucleophilic substitution reactions. The compound may exhibit moderate to high polarity due to the sulfonate group, affecting its solubility in various solvents. Additionally, the tetrahydropyran ring can provide a degree of flexibility and steric hindrance, which may impact its reactivity and interactions in chemical processes. Overall, this compound could be of interest in synthetic organic chemistry, particularly in the development of intermediates or in the synthesis of more complex molecules.
Formula:C13H18O4S
InChI:InChI=1/C13H18O4S/c1-11-2-4-13(5-3-11)18(14,15)17-10-12-6-8-16-9-7-12/h2-5,12H,6-10H2,1H3
SMILES:Cc1ccc(cc1)S(=O)(=O)OCC1CCOCC1
Synonyms:
  • (Tetrahydro-2H-pyran-4-yl)methyl tosylate
  • (Tetrahydro-2H-pyran-4-yl)methyl 4-methylbenzenesulphonate 98%
  • (Tetrahydro-2H-pyran-4-yl)methyl 4-methylbenzenesulfonate
  • (Tetrahydropyran-4-yl)methyl tosylate
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