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CAS 260367-12-2

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5-(9-Fluorenylmethyloxycarbonylamino)-3-oxapentanoic acid

Description:
5-(9-Fluorenylmethyloxycarbonylamino)-3-oxapentanoic acid, commonly referred to as Fmoc-3-oxapentanoic acid, is a chemical compound often utilized in peptide synthesis and bioconjugation. It features a fluorenylmethyloxycarbonyl (Fmoc) protecting group, which is widely used to protect amino groups during the synthesis of peptides. The presence of the oxapentanoic acid moiety indicates that it contains an ether linkage within a five-carbon chain, contributing to its structural complexity. This compound is typically a white to off-white solid and is soluble in organic solvents such as dimethyl sulfoxide (DMSO) and dimethylformamide (DMF), but may have limited solubility in water. Its molecular structure allows for the selective protection and deprotection of amino acids, making it valuable in the field of organic chemistry and peptide research. Additionally, the Fmoc group can be removed under mild basic conditions, facilitating the synthesis of peptides with desired sequences. Overall, this compound plays a crucial role in the development of peptide-based therapeutics and research applications.
Formula:C19H19NO5
InChI:InChI=1/C19H19NO5/c21-18(22)12-24-10-9-20-19(23)25-11-17-15-7-3-1-5-13(15)14-6-2-4-8-16(14)17/h1-8,17H,9-12H2,(H,20,23)(H,21,22)
SMILES:c1ccc2c(c1)c1ccccc1C2COC(=NCCOCC(=O)O)O
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