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CAS 1446282-39-8

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1,1-Dimethylethyl 3-[2-[2-(2-mercaptoethoxy)ethoxy]ethoxy]propanoate

Description:
1,1-Dimethylethyl 3-[2-[2-(2-mercaptoethoxy)ethoxy]ethoxy]propanoate, with the CAS number 1446282-39-8, is a chemical compound characterized by its complex structure, which includes multiple ether linkages and a mercapto group. This compound features a tert-butyl group, which contributes to its hydrophobic properties, and a propanoate moiety that may impart ester-like characteristics. The presence of the mercaptoethoxy groups suggests potential reactivity, particularly in nucleophilic substitution reactions, due to the thiol (-SH) functionality. This compound may exhibit solubility in organic solvents, while its polar ether groups could enhance its interaction with aqueous environments. Its unique structure may also influence its biological activity, making it of interest in various fields, including medicinal chemistry and materials science. Overall, the compound's properties are dictated by its functional groups, molecular weight, and steric effects, which can affect its reactivity and interactions in different chemical contexts.
Formula:C13H26O5S
InChI:InChI=1S/C13H26O5S/c1-13(2,3)18-12(14)4-5-15-6-7-16-8-9-17-10-11-19/h19H,4-11H2,1-3H3
InChI key:InChIKey=JLMCOVSNILLDKP-UHFFFAOYSA-N
SMILES:C(CCOCCOCCOCCS)(OC(C)(C)C)=O
Synonyms:
  • Propanoic acid, 3-[2-[2-(2-mercaptoethoxy)ethoxy]ethoxy]-, 1,1-dimethylethyl ester
  • 1,1-Dimethylethyl 3-[2-[2-(2-mercaptoethoxy)ethoxy]ethoxy]propanoate
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