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Home  > Nalpha-[(9h-fluoren-9-ylmethoxy)carbonyl]-l-threonine tert-butyl ester

AB76994

120791-76-6 | Nalpha-[(9h-fluoren-9-ylmethoxy)carbonyl]-l-threonine tert-butyl ester

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $42.00 $29.00 -   +
5g 98% in stock $156.00 $109.00 -   +
10g 98% in stock $276.00 $193.00 -   +
25g 98% in stock $516.00 $361.00 -   +
100g 98% in stock $1,550.00 $1,085.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB76994
Chemical Name: Nalpha-[(9h-fluoren-9-ylmethoxy)carbonyl]-l-threonine tert-butyl ester
CAS Number: 120791-76-6
Molecular Formula: C23H27NO5
Molecular Weight: 397.4642
MDL Number: MFCD08276378
SMILES: O=C(N[C@H](C(=O)OC(C)(C)C)[C@H](O)C)OCC1c2ccccc2-c2c1cccc2

 

Upstream Synthesis Route
  • Fmoc-Thr-OtBu, also known as Fmoc-protected threonine with t-butyl ester, is a widely used building block in chemical synthesis, particularly in solid-phase peptide synthesis (SPPS). This compound serves as an essential component for the controlled and efficient assembly of peptides and small proteins.In chemical synthesis, Fmoc-Thr-OtBu acts as a key intermediate for introducing threonine residues into peptide chains. The Fmoc (9-fluorenylmethoxycarbonyl) group serves as a temporary protective group, allowing for selective deprotection and subsequent coupling reactions during peptide elongation. The t-butyl ester moiety ensures stability and protection of the threonine amino acid until required for further manipulation in the synthesis process.By leveraging the versatility and reactivity of Fmoc-Thr-OtBu, chemists can systematically construct complex peptide sequences with precise control over the peptide bond formation. This strategic use of Fmoc-Thr-OtBu facilitates the stepwise assembly of peptides with specific sequences and functionalities, enabling the synthesis of bioactive peptides, pharmaceuticals, and peptide-based materials with high purity and efficiency.Moreover, the application of Fmoc-Thr-OtBu in chemical synthesis extends to the modification and functionalization of peptides for structure-activity relationship studies, drug development, and bioconjugation strategies. Its compatibility with modern peptide synthesis techniques makes Fmoc-Thr-OtBu an indispensable tool for researchers and chemists working in the field of peptide chemistry and drug discovery.
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