Tert-butyloxycarbonylamino-(2-methoxy-phenyl)-acetic acid, commonly referred to as Boc-amino acid, is an organic compound characterized by the presence of a tert-butyloxycarbonyl (Boc) protecting group attached to an amino acid structure. This compound features a methoxy-substituted phenyl group, which contributes to its aromatic properties and may 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 this compound can participate in various chemical reactions, including peptide synthesis and coupling reactions. Its solubility is typically influenced by the polar methoxy group and the overall structure, making it suitable for use in various organic synthesis applications. Additionally, the compound's stability under standard laboratory conditions is a key characteristic, although it may be sensitive to strong acids or bases that can cleave the Boc protecting group.

TERT-BUTOXYCARBONYLAMINO-(2-METHOXY-PHENYL)-ACETIC ACID

179417-69-7: Tert-butyloxycarbonylamino-(2-methoxy-phenyl)-acetic acid, commonly referred to as Boc-amino acid, is an organic compound characterized by the presence of a tert-butyloxycarbonyl (Boc) protecting group attached to an amino acid structure. This compound features a methoxy-substituted phenyl group, which contributes to its aromatic properties and may 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 this compound can participate in various chemical reactions, including peptide synthesis and coupling reactions. Its solubility is typically influenced by the polar methoxy group and the overall structure, making it suitable for use in various organic synthesis applications. Additionally, the compound's stability under standard laboratory conditions is a key characteristic, although it may be sensitive to strong acids or bases that can cleave the Boc protecting group.

CAS 179417-69-7

TERT-BUTOXYCARBONYLAMINO-(2-METHOXY-PHENYL)-ACETIC ACID

Benzeneacetic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-2-methoxy-

Ref: IN-DA002708

Boc-DL-(2-methoxyphenyl)glycine

Ref: 3D-EHA41769