![trans-4-[(R)-1-[(tert-Butyloxycarbonyl)amino]ethyl]cyclohexanecarboxylic acid](https://www.chemshuttle.com/media/catalog/product/cache/31dbf0bffbfa69a5826a72cec9a446de/1/9/195922_2.jpg)
(1R,3S)-3-aminocyclohexanecarboxylic acid
$200.00
CAS No.: 16636-51-4
Catalog No.: 196753
Purity: 95%
MF: C7H13NO2
MW: 143.186
Storage: 2-8 degree Celsius
SMILES: N[C@@H]1C[C@@H](CCC1)C(=O)O
Catalog No.: 196753
Purity: 95%
MF: C7H13NO2
MW: 143.186
Storage: 2-8 degree Celsius
SMILES: N[C@@H]1C[C@@H](CCC1)C(=O)O
(1R,3S)-3-aminocyclohexanecarboxylic acid; CAS No.: 16636-51-4; (1R,3S)-3-aminocyclohexanecarboxylic acid. PROPERTIES: This chiral amino-substituted cyclohexanecarboxylic acid features molecular formula C?H??NO? with molecular weight 143.19 g/mol. It generally appears as a white crystalline powder. Soluble in polar protic solvents like methanol and water. Melting point approximately 140-145 C. Exhibits IR absorption for carboxylic acid (~2900-2500 cm??) and amine groups (~3300-3000 cm??). Thermogravimetric analysis reveals weight loss onset above 180 C under nitrogen. For optimal stability, store at 2-8 C in tightly sealed containers with desiccant, protected from light. The compound may cause mild skin irritation and serious eye damage; therefore, standard laboratory safety precautions including protective clothing and eye protection are recommended during handling. APPLICATIONS: As a chiral amino acid, (1R,3S)-3-aminocyclohexanecarboxylic acid is predominantly utilized in the synthesis of peptide-based therapeutics. It serves as a key building block for constructing bioactive peptides with enhanced conformational stability, particularly in the development of enzyme inhibitors targeting metalloproteases (Journal of Medicinal Chemistry). Additionally, the compound participates in the development of fluorescent probes for bioimaging applications, where its amino acid functionality enables conjugation to biomolecules via amide bond formation (Bioconjugate Chemistry). In materials science, it functions as a monomer for preparing polyamino acid hydrogels with tunable mechanical properties, where the cyclohexane ring influences gelation behavior and biocompatibility (Biomacromolecules).
Reviews
Write Your Own Review