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CAS 946727-62-4

:

(4-Fmoc-amino-tetrahydrothiopyran-4-yl)-acetic acid

Description:
(4-Fmoc-amino-tetrahydrothiopyran-4-yl)-acetic acid is a chemical compound characterized by its unique structure, which includes a tetrahydrothiopyran ring and a Fmoc (9-fluorenylmethoxycarbonyl) protecting group. This compound is primarily used in peptide synthesis and other organic synthesis applications due to its ability to protect amino groups during reactions. The presence of the tetrahydrothiopyran moiety contributes to its potential biological activity, as this structure can influence the compound's interaction with biological targets. The acetic acid functional group provides acidity and can participate in various chemical reactions, enhancing the compound's versatility. Additionally, the Fmoc group is widely utilized in solid-phase peptide synthesis, allowing for the selective deprotection of amino acids. Overall, this compound's characteristics make it valuable in medicinal chemistry and the development of pharmaceutical agents. Its specific properties, such as solubility and reactivity, can vary based on the surrounding conditions and the presence of other functional groups in a synthetic pathway.
Formula:C22H23NO4S
Synonyms:
  • (4-Fmoc-amino-tetrahydrothiopyran-4-yl)-acetic acid
  • [4-({[(9H-Fluoren-9-yl)methoxy]carbonyl}amino)tetrahydro-2H-thiopyran-4-yl]acetic acid
  • 2H-Thiopyran-4-acetic acid, 4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]tetrahydro-
  • (9H-Fluoren-9-yl)methyl [4-(carboxymethyl)tetrahydro-2H-thiopyran-4-yl]carbamate, 4-Amino-4-(carboxymethyl)tetrahydro-2H-thiopyran, N-FMOC protected
  • 2-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)thian-4-yl]acetic acid
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