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172525-85-8

(2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-hydroxybutanoic acid

Catalog#: AR01DZJX  |   CAS#: 172525-85-8  |   MDL#: MFCD02682651  |   MF: C19H19NO5  |   MW: 341.3579

Packsize Purity Price Availability Quantity
100mg 96% $8.00 Global Stock Buy Now Add To Cart
250mg 96% $9.00 Global Stock Buy Now Add To Cart
1g 96% $14.00 Global Stock Buy Now Add To Cart
5g 96% $45.00 Global Stock Buy Now Add To Cart
25g 96% $162.00 Global Stock Buy Now Add To Cart
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Catalog Number AR01DZJX
Chemical Name (2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-hydroxybutanoic acid
CAS Number 172525-85-8
Molecular Formula C19H19NO5
Molecular Weight 341.3579
MDL Number MFCD02682651
SMILES OCC[C@@H](C(=O)O)NC(=O)OCC1c2ccccc2c2c1cccc2

N-Fmoc-L-homoserine is a versatile amino acid derivative commonly utilized in chemical synthesis for various applications. As a key building block in peptide synthesis, N-Fmoc-L-homoserine is crucial for the creation of complex peptide structures in the laboratory setting. Its Fmoc (Fluorenylmethyloxycarbonyl) protecting group provides stability during the synthesis process, facilitating the selective deprotection of the amino group when needed. This compound is particularly useful in solid-phase peptide synthesis, where the Fmoc protecting group strategy is commonly employed for sequential amino acid incorporation. Additionally, N-Fmoc-L-homoserine can be utilized in the development of pharmaceuticals, natural product synthesis, and in the study of protein structure and function. Its strategic incorporation into peptide sequences allows for the manipulation of peptide properties, enabling the exploration of structure-activity relationships and the creation of novel peptide-based materials. Overall, N-Fmoc-L-homoserine serves as a valuable tool in chemical synthesis, enabling the precise construction of peptides with diverse functionalities and applications.
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