Boc-L-Aha-OH*CHA, with the CAS number 120042-08-2, is a chemical compound that features a protected amino acid structure. The "Boc" (tert-butyloxycarbonyl) group serves as a protective moiety for the amino group, which is commonly used in peptide synthesis to prevent unwanted reactions. The "L-Aha" refers to L-α-amino-3-hydroxy-5-aminopentanoic acid, indicating that this compound contains an amino acid with a hydroxyl group, contributing to its potential reactivity and solubility in various solvents. The "OH" denotes the presence of a hydroxyl group, which can participate in hydrogen bonding and influence the compound's polarity. The "CHA" likely refers to a specific side chain or additional functional group that may enhance the compound's biological activity or stability. Overall, Boc-L-Aha-OH*CHA is utilized in peptide synthesis and research, particularly in the development of pharmaceuticals and biologically active compounds, due to its structural features that facilitate various chemical reactions.

Boc-L-Aha-OH*CHA

120042-08-2: Boc-L-Aha-OH*CHA, with the CAS number 120042-08-2, is a chemical compound that features a protected amino acid structure. The "Boc" (tert-butyloxycarbonyl) group serves as a protective moiety for the amino group, which is commonly used in peptide synthesis to prevent unwanted reactions. The "L-Aha" refers to L-α-amino-3-hydroxy-5-aminopentanoic acid, indicating that this compound contains an amino acid with a hydroxyl group, contributing to its potential reactivity and solubility in various solvents. The "OH" denotes the presence of a hydroxyl group, which can participate in hydrogen bonding and influence the compound's polarity. The "CHA" likely refers to a specific side chain or additional functional group that may enhance the compound's biological activity or stability. Overall, Boc-L-Aha-OH*CHA is utilized in peptide synthesis and research, particularly in the development of pharmaceuticals and biologically active compounds, due to its structural features that facilitate various chemical reactions.

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CAS 120042-08-2

Boc-L-Aha-OH*CHA

N-α-Boc-Nγ-Azido-L-2,4-diaminobutyric acid cyclohexylamine salt

Ref: 3D-FB57246

Butanoic acid, 4-azido-2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (2S)-

Ref: IN-DA000Q76