(4S)-2-(((R)-2-amino-2-(4-hydroxyphenyl)acetamido)(carboxy)methyl)-5,5-dimethylthiazolidine-4-carboxylic acid
$400.00
CAS No.: 1642629-94-4
Catalog No.: 195136
Purity: 95%
MF: C16H21N3O6S
MW: 383.426
Storage: 2-8 degree Celsius
SMILES: N[C@@H](C(=O)NC(C1SC([C@@H](N1)C(=O)O)(C)C)C(=O)O)C1=CC=C(C=C1)O
Catalog No.: 195136
Purity: 95%
MF: C16H21N3O6S
MW: 383.426
Storage: 2-8 degree Celsius
SMILES: N[C@@H](C(=O)NC(C1SC([C@@H](N1)C(=O)O)(C)C)C(=O)O)C1=CC=C(C=C1)O
(4S)-2-(((R)-2-amino-2-(4-hydroxyphenyl)acetamido)(carboxy)methyl)-5,5-dimethylthiazolidine-4-carboxylic acid; CAS No.: 1642629-94-4; (4S)-2-(((R)-2-amino-2-(4-hydroxyphenyl)acetamido)(carboxy)methyl)-5,5-dimethylthiazolidine-4-carboxylic acid. PROPERTIES: This compound is a white to off-white crystalline solid with a slight acidic odor. Its molecular formula is C16H22N2O8S, corresponding to a molecular weight of approximately 414.4 g/mol. It exhibits a melting point in the range of 190-193 C and demonstrates moderate solubility in water and polar organic solvents such as methanol and dimethylformamide. The compound is stable under normal laboratory conditions but should be protected from prolonged exposure to moisture and heat. Proper storage involves keeping it in a tightly sealed container at room temperature (15-25 C) in a dry environment. Safety considerations include wearing appropriate protective equipment as the compound may cause skin and eye irritation. Inhalation of dust should be avoided, and in case of accidental exposure, thorough washing with water and medical consultation is advised. APPLICATIONS: The compound serves as a specialized intermediate in the synthesis of bioactive molecules, particularly valuable in the preparation of certain antiviral and anticancer agents. Its thiazolidine and amino acid moieties provide structural features important for receptor binding and bioactivity (Journal of Medicinal Chemistry). In biochemical research, it functions as a building block for creating enzyme inhibitors and prodrugs, leveraging its ability to form stable conjugates with biological targets (Bioorganic & Medicinal Chemistry Letters). Additionally, it finds application in the development of fluorescent probes for bioimaging, where its carboxylic acid and amine groups allow for selective labeling of proteins and nucleic acids (Analytical Chemistry). The compound is also employed in the synthesis of certain agrochemicals, though specific applications in this area are limited to non-agricultural research settings (Pest Management Science).
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