Tert-butyl (4R)-4,5-diamino-5-oxopentanoate, identified by its CAS number 70701-78-9, is an organic compound characterized by its structure, which includes a tert-butyl group and a pentanoate moiety featuring both amino and keto functional groups. This compound is typically a white to off-white solid, soluble in polar solvents such as water and alcohols, due to the presence of amino groups that can engage in hydrogen bonding. The presence of the tert-butyl group contributes to its hydrophobic character, influencing its solubility and reactivity. The compound is often studied in the context of pharmaceuticals and biochemistry, particularly for its potential applications in drug development and as a building block in peptide synthesis. Its chiral center at the 4-position indicates that it can exist in different stereoisomeric forms, which may exhibit distinct biological activities. As with many amino acid derivatives, it may participate in various chemical reactions, including acylation and amidation, making it a versatile intermediate in organic synthesis.

tert-butyl (4R)-4,5-diamino-5-oxopentanoate

70701-78-9: Tert-butyl (4R)-4,5-diamino-5-oxopentanoate, identified by its CAS number 70701-78-9, is an organic compound characterized by its structure, which includes a tert-butyl group and a pentanoate moiety featuring both amino and keto functional groups. This compound is typically a white to off-white solid, soluble in polar solvents such as water and alcohols, due to the presence of amino groups that can engage in hydrogen bonding. The presence of the tert-butyl group contributes to its hydrophobic character, influencing its solubility and reactivity. The compound is often studied in the context of pharmaceuticals and biochemistry, particularly for its potential applications in drug development and as a building block in peptide synthesis. Its chiral center at the 4-position indicates that it can exist in different stereoisomeric forms, which may exhibit distinct biological activities. As with many amino acid derivatives, it may participate in various chemical reactions, including acylation and amidation, making it a versatile intermediate in organic synthesis.

(R)-tert-Butyl 4,5-diamino-5-oxopentanoate

CAS 70701-78-9

tert-butyl (4R)-4,5-diamino-5-oxopentanoate

(R)-tert-Butyl 4,5-diamino-5-oxopentanoate

Ref: 54-OR1052339