(1S,2R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclohexanecarboxylic acid
$225.00
CAS No.: 430460-38-1
Catalog No.: 193250
Purity: 95%
MF: C22H23NO4
MW: 365.429
Storage: 2-8 degree Celsius
SMILES: C1=CC=CC=2C3=CC=CC=C3C(C12)COC(=O)N[C@H]1[C@H](CCCC1)C(=O)O
Catalog No.: 193250
Purity: 95%
MF: C22H23NO4
MW: 365.429
Storage: 2-8 degree Celsius
SMILES: C1=CC=CC=2C3=CC=CC=C3C(C12)COC(=O)N[C@H]1[C@H](CCCC1)C(=O)O
(1S,2R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclohexanecarboxylic acid; CAS No.: 430460-38-1; (1S,2R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclohexanecarboxylic acid. PROPERTIES: This compound is a (1S,2R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclohexanecarboxylic acid appearing as white crystalline powder. Its molecular weight is approximately 473.50 g/mol. It has melting point around 145-150 C. The compound is moderately soluble in common organic solvents like dimethylformamide. It's moisture sensitive and may hydrolyze upon exposure to atmospheric moisture. Store in tightly sealed containers under nitrogen atmosphere. Keep below 25 C and protect from moisture. Handle with care using appropriate protective equipment when handling powder. APPLICATIONS: (1S,2R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclohexanecarboxylic acid is utilized in organic synthesis as fluorenylmethoxycarbonyl-protected aminocyclohexyl building block as detailed in Journal of Organic Chemistry. It's employed in preparation of certain anticonvulsant agents mentioned in Journal of Medicinal Chemistry. Additionally, this compound serves as intermediate for synthesizing fluorenylmethoxycarbonyl-protected aminocyclohexyl-containing pharmaceuticals reported in Organic Process Research & Development. The fluorenylmethoxycarbonyl group provides valuable temporary protection for amine functionality during multi-step synthesis.
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