The chemical substance known as (2R)-2-(tert-butoxycarbonylamino)-3-(3-chloro-4-hydroxy-phenyl)propanoic acid, with the CAS number 478183-57-2, is an amino acid derivative characterized by its complex structure that includes a tert-butoxycarbonyl (Boc) protecting group, an amino group, and a phenyl ring substituted with a chlorine and hydroxyl group. This compound typically exhibits properties associated with amino acids, such as the ability to form hydrogen bonds due to the presence of the hydroxyl group and the amino functionality. The presence of the Boc group suggests that it is likely used in peptide synthesis, as this protecting group can be removed under specific conditions to reveal the free amine. The chloro and hydroxy substituents on the phenyl ring may impart unique reactivity and solubility characteristics, making it potentially useful in medicinal chemistry or as a building block in organic synthesis. Overall, this compound's structure suggests it may have applications in pharmaceuticals or biochemistry, particularly in the development of peptide-based therapeutics.

(2R)-2-(tert-butoxycarbonylamino)-3-(3-chloro-4-hydroxy-phenyl)propanoic acid

478183-57-2: The chemical substance known as (2R)-2-(tert-butoxycarbonylamino)-3-(3-chloro-4-hydroxy-phenyl)propanoic acid, with the CAS number 478183-57-2, is an amino acid derivative characterized by its complex structure that includes a tert-butoxycarbonyl (Boc) protecting group, an amino group, and a phenyl ring substituted with a chlorine and hydroxyl group. This compound typically exhibits properties associated with amino acids, such as the ability to form hydrogen bonds due to the presence of the hydroxyl group and the amino functionality. The presence of the Boc group suggests that it is likely used in peptide synthesis, as this protecting group can be removed under specific conditions to reveal the free amine. The chloro and hydroxy substituents on the phenyl ring may impart unique reactivity and solubility characteristics, making it potentially useful in medicinal chemistry or as a building block in organic synthesis. Overall, this compound's structure suggests it may have applications in pharmaceuticals or biochemistry, particularly in the development of peptide-based therapeutics.

CAS 478183-57-2

(2R)-2-(tert-butoxycarbonylamino)-3-(3-chloro-4-hydroxy-phenyl)propanoic acid

Boc-3-chloro-d-tyrosine dicyclohexylamine salt

Ref: IN-DA00D94S

(R)-2-((tert-butoxycarbonyl)amino)-3-(3-chloro-4-hydroxyphenyl)propanoic acid

Ref: 10-F774017