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CAS 946716-25-2

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

Description:
(4-Fmoc-amino-tetrahydropyran-4-yl)-acetic acid is a chemical compound characterized by its unique structure, which includes a tetrahydropyran ring and a Fmoc (9-fluorenylmethoxycarbonyl) protecting group. This compound is typically used in peptide synthesis and other organic synthesis applications due to its ability to protect amino groups during reactions. The presence of the acetic acid moiety contributes to its solubility in polar solvents, making it suitable for various chemical reactions. The Fmoc group is particularly advantageous for its stability under basic conditions and ease of removal under mild acidic conditions, allowing for selective deprotection in multi-step synthesis. Additionally, the tetrahydropyran ring provides a cyclic structure that can influence the compound's reactivity and steric properties. Overall, (4-Fmoc-amino-tetrahydropyran-4-yl)-acetic acid is a valuable intermediate in the field of medicinal chemistry and peptide research, facilitating the development of complex molecules.
Formula:C22H23NO5
Synonyms:
  • [4-({{(9H-Fluoren-9-yl)methoxy]carbonyl}amino)tetrahydro-2H-pyran-4-yl]acetic acid
  • (4-Fmoc-amino-tetrahydropyran-4-yl)-acetic acid
  • (9H-Fluoren-9-yl)methyl [4-(carboxymethyl)tetrahydro-2H-pyran-4-yl]carbamate, 4-Amino-4-(carboxymethyl)tetrahydro-2H-pyran, N-FMOC protected
  • 2-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)oxan-4-yl]acetic acid
  • 2H-Pyran-4-acetic acid, 4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]tetrahydro-
  • (Fmoc-NH-THP)acetic acid
  • N-Fmoc-2-(4-Aminooxan-4-yl)acetic acid
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