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CAS 182287-49-6

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TERT-BUTOXYCARBONYLAMINO-(TETRAHYDRO-PYRAN-4-YL)-ACETIC ACID

Description:
Tert-butyloxycarbonylamino-(tetrahydro-pyran-4-yl)-acetic acid, commonly referred to as Boc-amino acid, is a chemical compound characterized by its structure that includes a tert-butyloxycarbonyl (Boc) protecting group attached to an amino acid derivative. This compound features a tetrahydropyran ring, which contributes to its cyclic structure and can influence its reactivity and solubility. The Boc group is widely used in organic synthesis as a protective group for amines, allowing for selective reactions without interfering with the amino functionality. The presence of the acetic acid moiety indicates that it has acidic properties, which can be relevant in various chemical reactions. This compound is typically utilized in peptide synthesis and other organic transformations, where the protection and subsequent deprotection of the amino group are crucial steps. Its stability under basic conditions and reactivity under acidic conditions make it a valuable intermediate in synthetic chemistry. Overall, this compound is significant in the field of medicinal chemistry and peptide synthesis due to its functional versatility.
Formula:C12H21NO5
InChI:InChI=1/C12H21NO5/c1-12(2,3)18-11(16)13-9(10(14)15)8-4-6-17-7-5-8/h8-9H,4-7H2,1-3H3,(H,13,16)(H,14,15)
SMILES:CC(C)(C)OC(=NC(C1CCOCC1)C(=O)O)O
Synonyms:
  • N-Boc-2-(Tetrahydro-Pyran-4-Yl)-Glycine
  • N-Boc-4'-Tetrahydropyranylglycine
  • [(tert-butoxycarbonyl)amino](tetrahydro-2H-pyran-4-yl)acetic acid
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