CAS 6367-11-9: Ac-His-NHMe
Formula:C9H14N4O2
InChI:InChI=1/C9H14N4O2/c1-6(14)13-8(9(15)10-2)3-7-4-11-5-12-7/h4-5,8H,3H2,1-2H3,(H,10,15)(H,11,12)(H,13,14)/t8-/m0/s1
SMILES:CC(=N[C@@H](Cc1cnc[nH]1)C(=NC)O)O
Synonyms:- 1H-Imidazole-4-propanamide, alpha-(acetylamino)-N-methyl-, (S)-
- (S)-alpha-(Acetylamino)-N-methyl-1H-imidazole-4-propanamide
- Nalpha-acetyl-N-methyl-L-histidinamide
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Found 5 products.
N-Acetyl-L-histidine methyl amide
CAS:N-Acetyl-L-histidine methyl amide is a histidine derivative that has an acidic residue. It is also a transition metal ion, which can form complexes with macroscopic and aromatic residues. N-Acetyl-L-histidine methyl amide binds to protonated histidines in tripeptides, forming a covalent bond. This reaction is stereoselective and the protonated nitrogen atom can be protonated or deprotonated, depending on the solvent polarity. N-Acetyl-L-histidine methyl amide oxidizes to produce an ionizable group when exposed to air, making it suitable for structural studies in nonpolar solvents.Formula:C9H14N4O2Purity:Min. 95%Color and Shape:PowderMolecular weight:210.23 g/molRef: 3D-FA48138
Discontinued productAc-His-NHMe
CAS:Bachem ID: 4017306.Formula:C9H14N4O2Purity:> 99%Color and Shape:White PowderMolecular weight:210.24N-Acetyl-L-histidine Methylamide
CAS:Controlled ProductApplications N-Acetyl-L-histidine Methylamide is used in the synthesis of peptide. References Minamino, N., et al.: Peptide Chem., 15, 85 (1978),Formula:C9H14N4O2Color and Shape:NeatMolecular weight:210.23
