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AB74332

111061-56-4 | Fmoc-Ser(Trt)-OH

Packsize Purity Availability Price Discounted Price    Quantity
1g 96% in stock $16.00 $11.00 -   +
5g 96% in stock $23.00 $16.00 -   +
10g 96% in stock $36.00 $25.00 -   +
25g 96% in stock $68.00 $47.00 -   +
100g 96% in stock $206.00 $144.00 -   +
500g 96% in stock $914.00 $640.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB74332
Chemical Name: Fmoc-Ser(Trt)-OH
CAS Number: 111061-56-4
Molecular Formula: C37H31NO5
Molecular Weight: 569.64574
MDL Number: MFCD00153364
SMILES: O=C(N[C@H](C(=O)O)COC(c1ccccc1)(c1ccccc1)c1ccccc1)OCC1c2ccccc2-c2c1cccc2

 

Computed Properties
Complexity: 837  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 43  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 11  
XLogP3: 7.2  

 

 

Upstream Synthesis Route
  • Fmoc-Ser(Trt)-OH is a key building block widely used in chemical synthesis, particularly in the field of peptide synthesis. This compound serves as a protected form of serine amino acid, allowing for selective incorporation into peptide chains during solid-phase peptide synthesis. By utilizing the Fmoc (9-fluorenylmethyloxycarbonyl) protecting group along with the Trt (trityl) protecting group on the serine residue, Fmoc-Ser(Trt)-OH enables efficient and controlled peptide bond formation. This strategy offers chemists the flexibility to introduce serine residues at specific locations within the peptide sequence, leading to the synthesis of complex peptides with high purity and yield. Additionally, the Fmoc protecting group can be readily removed under mild conditions, unveiling the reactive serine functionality for subsequent synthetic steps. In summary, Fmoc-Ser(Trt)-OH plays a crucial role in the precise assembly of peptides with diverse biological activities and structural motifs.
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