Boc-His(1-Me)-OH, also known as Boc-protected 1-methylhistidine, is a derivative of the amino acid histidine, characterized by the presence of a tert-butyloxycarbonyl (Boc) protecting group on the amino group and a methyl group at the 1-position of the imidazole ring. This compound is typically used in peptide synthesis and biochemistry due to its ability to protect the amino group during reactions, allowing for selective modifications of other functional groups. The Boc group is easily removable under acidic conditions, facilitating the subsequent deprotection of the amino group when needed. The presence of the methyl group at the 1-position can influence the compound's steric and electronic properties, potentially affecting its reactivity and interactions in biological systems. Boc-His(1-Me)-OH is soluble in organic solvents and exhibits stability under standard laboratory conditions, making it a valuable intermediate in the synthesis of peptides and other bioactive molecules. Its unique structure allows for specific applications in drug design and development, particularly in the context of histidine-containing peptides.

Boc-His(1-Me)-OH

61070-20-0: N-Boc-N-Im-1-Methyl-L-Histidine, Boc-His(Nt-Me)-OH

Boc-His(1-Me)-OH  Boc-His(t-Me)-OH

BOC-HIS(1-ME)-OH

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CAS 61070-20-0: Boc-His(1-Me)-OH

Boc-His(1-Me)-OH Boc-His(t-Me)-OH

Ref: 54-OR36466

BOC-HIS(1-ME)-OH

Ref: IN-DA00EGQS

Boc-His(1-Me)-OH

Ref: 3D-FB47490

BOC-HIS(1-ME)-OH

Ref: 10-F475409