Z-HIS-OME, also known as Z-Histidine methyl ester, is a derivative of the amino acid histidine. It is characterized by the presence of a Z (benzyloxycarbonyl) protecting group on the amino group and a methyl ester at the carboxylic acid end. This compound is typically used in peptide synthesis and as an intermediate in the production of various bioactive molecules. Z-HIS-OME is soluble in polar organic solvents, which facilitates its use in various chemical reactions. The presence of the histidine moiety imparts unique properties, such as the ability to participate in coordination chemistry due to the imidazole side chain, which can act as a ligand for metal ions. Additionally, the Z protecting group allows for selective deprotection under specific conditions, making it a valuable tool in synthetic organic chemistry. Overall, Z-HIS-OME serves as an important building block in the synthesis of peptides and other complex organic compounds.

Z-HIS-OME

15545-10-5: N-Alpha-Cbz-L-Histidine Methyl Ester, N-Alpha-Carbobenzoxy-L-Histidine Methyl Ester, Z-L-Histidine Methyl Ester

Na-Z-L-histidine methyl ester is a solvent that is used in the synthesis of peptides. It is a low water, hydrophobic, and thermodynamically stable liquid that is soluble in dimethylformamide. Na-Z-L-histidine methyl ester is also an amide with a trifluoroacetic acid group and can be used to synthesize solid phase peptides. The compound has been shown to have thyrotropin releasing effects on rats when administered intravenously.

CAS 15545-10-5: Z-HIS-OME

Na-Z-L-histidine methyl ester

Ref: 3D-FN47836

Z-HIS-OME

Ref: IN-DA00AB93

Na-Z-L-histidine methyl ester

Ref: 10-F492706