H-Ala-p-nitrobenzyl ester·HBr, with the CAS number 10144-66-8, is a chemical compound that features an alanine amino acid derivative. This substance is characterized by the presence of a p-nitrobenzyl ester group, which contributes to its unique properties, including its potential use in peptide synthesis and as a protecting group in organic chemistry. The hydrochloride (HBr) indicates that the compound is in its salt form, which enhances its solubility in polar solvents, making it suitable for various chemical reactions. The p-nitrobenzyl moiety is known for its ability to undergo photolytic cleavage, making it useful in photochemistry and drug delivery systems. Additionally, the compound may exhibit biological activity due to the presence of the alanine residue, which is a non-polar, aliphatic amino acid. Overall, H-Ala-p-nitrobenzyl ester·HBr is a versatile compound with applications in synthetic organic chemistry and biochemistry.

H-Ala-p-nitrobenzyl ester . HBr

10144-66-8: H-Ala-p-nitrobenzyl ester·HBr, with the CAS number 10144-66-8, is a chemical compound that features an alanine amino acid derivative. This substance is characterized by the presence of a p-nitrobenzyl ester group, which contributes to its unique properties, including its potential use in peptide synthesis and as a protecting group in organic chemistry. The hydrochloride (HBr) indicates that the compound is in its salt form, which enhances its solubility in polar solvents, making it suitable for various chemical reactions. The p-nitrobenzyl moiety is known for its ability to undergo photolytic cleavage, making it useful in photochemistry and drug delivery systems. Additionally, the compound may exhibit biological activity due to the presence of the alanine residue, which is a non-polar, aliphatic amino acid. Overall, H-Ala-p-nitrobenzyl ester·HBr is a versatile compound with applications in synthetic organic chemistry and biochemistry.

CAS 10144-66-8

H-Ala-p-nitrobenzyl ester . HBr