Boc-N-Me-Thr-OH, also known as N-Boc-N-methyl-threonine, is a protected amino acid commonly used in peptide synthesis. The "Boc" (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, allowing for selective reactions without interfering with the amine. The "N-Me" indicates the presence of a methyl group attached to the nitrogen, which can influence the steric and electronic properties of the molecule. Threonine, the underlying amino acid, is characterized by its hydroxyl group, which contributes to its hydrophilicity and potential for hydrogen bonding. This compound is typically utilized in the synthesis of peptides where the protection of the amino group is necessary to prevent unwanted reactions during coupling processes. Its stability under various conditions makes it a valuable intermediate in organic synthesis and pharmaceutical applications. Additionally, the presence of the hydroxyl group in threonine can facilitate further modifications or conjugations, expanding its utility in biochemistry and medicinal chemistry.

Boc-N-Me-Thr-OH

101759-72-2: Boc-N-Me-Thr-OH, also known as N-Boc-N-methyl-threonine, is a protected amino acid commonly used in peptide synthesis. The "Boc" (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, allowing for selective reactions without interfering with the amine. The "N-Me" indicates the presence of a methyl group attached to the nitrogen, which can influence the steric and electronic properties of the molecule. Threonine, the underlying amino acid, is characterized by its hydroxyl group, which contributes to its hydrophilicity and potential for hydrogen bonding. This compound is typically utilized in the synthesis of peptides where the protection of the amino group is necessary to prevent unwanted reactions during coupling processes. Its stability under various conditions makes it a valuable intermediate in organic synthesis and pharmaceutical applications. Additionally, the presence of the hydroxyl group in threonine can facilitate further modifications or conjugations, expanding its utility in biochemistry and medicinal chemistry.

CAS 101759-72-2

Boc-N-Me-Thr-OH

(2S,3R)-2-((tert-Butoxycarbonyl)(methyl)amino)-3-hydroxybutanoic acid

Ref: IN-DA0005EE