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CAS 61070-22-2

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N-[(1,1-Dimethylethoxy)carbonyl]-3-methyl-L-histidine

Description:
N-[(1,1-Dimethylethoxy)carbonyl]-3-methyl-L-histidine, with the CAS number 61070-22-2, is a chemical compound that belongs to the class of amino acids, specifically a derivative of histidine. This compound features a histidine backbone modified with a 1,1-dimethylethoxycarbonyl group at the nitrogen position, which enhances its stability and solubility in various solvents. The presence of the 3-methyl group on the histidine structure contributes to its unique properties, potentially influencing its biological activity and interactions. This compound is typically used in peptide synthesis and may serve as a building block in the development of pharmaceuticals or biochemicals. Its characteristics include a specific molecular weight, a defined melting point, and solubility in polar solvents, which are essential for its application in research and industry. As with many amino acid derivatives, it may exhibit specific optical activity due to its chiral centers, making it relevant in studies of stereochemistry and biological interactions.
Formula:C12H19N3O4
InChI:InChI=1S/C12H19N3O4/c1-12(2,3)19-11(18)14-9(10(16)17)5-8-6-13-7-15(8)4/h6-7,9H,5H2,1-4H3,(H,14,18)(H,16,17)/t9-/m0/s1
InChI key:InChIKey=BGZFLUIZBZNCTI-VIFPVBQESA-N
SMILES:C([C@H](NC(OC(C)(C)C)=O)C(O)=O)C=1N(C)C=NC1
Synonyms:
  • (2S)-2-[(tert-Butoxycarbonyl)amino]-3-(1-methyl-1H-imidazol-5-yl)propionic acid
  • (2S)-3-(3-Methylimidazol-4-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
  • <span class="text-smallcaps">L</span>-Histidine, N-[(1,1-dimethylethoxy)carbonyl]-3-methyl-
  • N-(tert-butoxycarbonyl)-3-methyl-L-histidine
  • N-[(1,1-Dimethylethoxy)carbonyl]-3-methyl-<span class="text-smallcaps">L</span>-histidine
  • N-[(Tert-Butoxy)Carbonyl]-3-Methyl-L-Histidine
  • L-Histidine, N-[(1,1-dimethylethoxy)carbonyl]-3-methyl-
  • N-[(1,1-Dimethylethoxy)carbonyl]-3-methyl-L-histidine
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