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73724-48-8

L-Threonine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, phenylmethyl ester

Catalog#: AR00FDM8  |   CAS#: 73724-48-8  |   MDL#: MFCD11505901  |   MF: C26H25NO5  |   MW: 431.4804

Packsize Purity Price Availability Quantity
1g 95% $15.00 Global Stock Buy Now Add To Cart
5g 95% $46.00 Global Stock Buy Now Add To Cart
10g 95% $62.00 Global Stock Buy Now Add To Cart
25g 95% $154.00 Global Stock Buy Now Add To Cart
100g 95% $616.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00FDM8
Chemical Name L-Threonine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, phenylmethyl ester
CAS Number 73724-48-8
Molecular Formula C26H25NO5
Molecular Weight 431.4804
MDL Number MFCD11505901
SMILES O=C(N[C@H](C(=O)OCc1ccccc1)[C@H](O)C)OCC1c2ccccc2-c2c1cccc2

Fmoc-Thr-Obzl is a key building block in chemical synthesis, particularly in the field of peptide synthesis. This compound, which consists of a threonine amino acid residue protected with Fmoc (9-fluorenylmethyloxycarbonyl) at the N-terminus and Obzl (2,2,5,7,8-pentamethylchroman-6-sulfonyl) at the side chain hydroxyl group, plays a crucial role in the stepwise assembly of peptides.In chemical synthesis, Fmoc-Thr-Obzl acts as a strategic component for introducing threonine residues into peptide chains. The Fmoc group serves to protect the amine group of threonine, preventing unwanted side reactions during the coupling steps. Additionally, the Obzl protecting group safeguards the hydroxyl group of threonine, ensuring selective deprotection and precise control over the peptide elongation process.By utilizing Fmoc-Thr-Obzl in peptide synthesis, chemists can achieve high yields, purity, and efficiency in constructing custom-designed peptides with specific sequences and functionalities. This compound enables the synthesis of complex peptides with precise stereochemistry, making it an invaluable tool in the creation of peptide-based drugs, biomolecules, and materials for various biomedical and chemical applications.
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