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AA10506

102747-84-2 | H-Gln(trt)-oh

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $15.00 $10.00 -   +
1g 95% in stock $16.00 $11.00 -   +
5g 95% in stock $42.00 $30.00 -   +
10g 95% in stock $73.00 $51.00 -   +
25g 95% in stock $123.00 $86.00 -   +
100g 95% in stock $435.00 $305.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA10506
Chemical Name: H-Gln(trt)-oh
CAS Number: 102747-84-2
Molecular Formula: C24H24N2O3
Molecular Weight: 388.459
MDL Number: MFCD00237060
SMILES: OC(=O)[C@@H](NC(c1ccccc1)(c1ccccc1)c1ccccc1)CCC(=O)N

 

Upstream Synthesis Route
  • H-Gln(Trt)-OH, also known as N-tert-butoxycarbonyl-L-glutamine, serves as a crucial building block in chemical synthesis due to its diverse applications. This compound, protected by a trityl group, is commonly used in peptide synthesis to introduce a glutamine residue into the peptide chain. Its unique properties make it an ideal starting material for the production of peptide-based drugs and pharmaceuticals.In chemical synthesis, H-Gln(Trt)-OH acts as a versatile intermediate, allowing chemists to selectively incorporate glutamine residues at specific positions within a peptide sequence. By deprotecting the trityl group under controlled conditions, it enables precise manipulation of the peptide structure while ensuring the desired chemical reactions occur with high efficiency. This process is crucial for the development of therapeutic peptides, which often require complex sequences for optimal biological activity.Furthermore, H-Gln(Trt)-OH plays a key role in the synthesis of peptidomimetics and other bioactive molecules where the presence of a glutamine moiety is essential for their function. Its ability to protect the glutamine side chain while facilitating peptide bond formation makes it an indispensable tool in the field of medicinal chemistry. Overall, H-Gln(Trt)-OH is a valuable reagent that contributes significantly to the advancement of chemical synthesis and the development of novel peptide-based therapeutics.
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