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(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propanoic acid
$300.00
CAS No.: 204058-25-3
Catalog No.: 194412
Purity: 95%
MF: C28H34N2O6
MW: 494.588
Storage: 2-8 degree Celsius
SMILES: C1=CC=CC=2C3=CC=CC=C3C(C12)COC(=O)N[C@H](C(=O)O)CC1CCN(CC1)C(=O)OC(C)(C)C
Catalog No.: 194412
Purity: 95%
MF: C28H34N2O6
MW: 494.588
Storage: 2-8 degree Celsius
SMILES: C1=CC=CC=2C3=CC=CC=C3C(C12)COC(=O)N[C@H](C(=O)O)CC1CCN(CC1)C(=O)OC(C)(C)C
(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propanoic acid; CAS No.: 204058-25-3; (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propanoic acid. PROPERTIES: (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propanoic acid is a crystalline solid. Its molecular formula is C28H32N2O6, and the molecular weight is approximately 500.57 g/mol. The compound has a melting point of approximately 130-132 C. It is moderately soluble in common organic solvents such as methanol and dimethylformamide, but is poorly soluble in water. For proper storage, it should be kept in a sealed container at room temperature, away from heat and direct sunlight. As a compound containing a fluorenylmethoxy carbonyl group, a tert-butoxycarbonyl group, and a piperidine ring, it may exhibit certain reactivity and stability. When handling it, protective gloves and eye protection should be worn. In case of accidental contact with skin or eyes, immediate rinsing with water is necessary. APPLICATIONS: In organic synthesis, this compound serves as a specialized intermediate. The fluorenylmethoxy carbonyl and tert-butoxycarbonyl groups provide opportunities for protecting and deprotecting amine groups. The piperidine ring offers opportunities for further functionalization. In the pharmaceutical industry, derivatives of this compound can be explored as potential drug candidates. For example, in the development of certain peptide-based drugs, the structure of this compound can be utilized to enhance the drug's stability and bioavailability (as reported in medicinal chemistry journals). Additionally, in the field of chemical research, it can be used as a starting material for the synthesis of novel organic compounds with potential applications in catalysis and sensing (as noted in organic chemistry research papers).
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