AB56073
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
5g | 97% | in stock | $17.00 | $12.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB56073 |
Chemical Name: | H-Glu(ochex)-oh |
CAS Number: | 112471-82-6 |
Molecular Formula: | C11H19NO4 |
Molecular Weight: | 229.2729 |
MDL Number: | MFCD00153436 |
SMILES: | N[C@H](C(=O)O)CCC(=O)OC1CCCCC1 |
H-Glu(OcHex)-OH, also known as hexyl ester of N-hexanoyl-DL-glutamic acid, is a versatile compound commonly used in chemical synthesis. This compound serves as a valuable building block in organic chemistry, specifically in the synthesis of peptides and other bioactive molecules.In chemical synthesis, H-Glu(OcHex)-OH is often employed as a protected form of glutamic acid. Its hexyl ester group provides protection to the glutamic acid moiety, allowing for selective reactions to occur at other functional groups within a molecule without affecting the glutamic acid residue. This protection strategy is crucial in the stepwise assembly of complex peptides and proteins, where precise control over the order of reactions is essential.Furthermore, the hexyl ester group in H-Glu(OcHex)-OH can be selectively removed under mild acidic conditions, yielding the free glutamic acid residue. This deprotection step is crucial for accessing the fully functionalized peptide or molecule, ready for further manipulation or biological activity studies.Overall, H-Glu(OcHex)-OH plays a fundamental role in the synthesis of peptides and bioactive molecules by offering protection to the glutamic acid residue and enabling precise control over chemical reactions. Its versatility and compatibility with common peptide synthesis strategies make it a valuable tool for organic chemists and researchers working in the field of chemical synthesis.