AE12808
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 97% | in stock | $26.00 | $18.00 | - + | |
5g | 97% | in stock | $34.00 | $24.00 | - + | |
25g | 97% | in stock | $62.00 | $44.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE12808 |
Chemical Name: | Boc-DL-Glu(Obzl)-OH |
CAS Number: | 117997-81-6 |
Molecular Formula: | C17H23NO6 |
Molecular Weight: | 337.3676 |
MDL Number: | MFCD00798612 |
SMILES: | O=C(OCc1ccccc1)CCC(C(=O)O)NC(=O)OC(C)(C)C |
Complexity: | 437 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 24 |
Hydrogen Bond Acceptor Count: | 6 |
Hydrogen Bond Donor Count: | 2 |
Rotatable Bond Count: | 10 |
Undefined Atom Stereocenter Count: | 1 |
XLogP3: | 2.2 |
Boc-DL-Glu(OBzl)-OH is a versatile building block in chemical synthesis, commonly used as a protected form of glutamic acid. This compound is utilized in peptide synthesis as a key intermediate for the preparation of complex peptides and peptidomimetics. By selectively protecting the amine and carboxylic acid groups with the Boc (tert-butyloxycarbonyl) and OBzl (benzyl ester) groups, respectively, Boc-DL-Glu(OBzl)-OH enables efficient peptide bond formation while preventing undesired side reactions. Its compatibility with common coupling reagents and deprotection methods makes it an essential tool for the synthesis of diverse peptide sequences with high purity and yield. Additionally, the Boc protection strategy allows for stepwise elongation of peptide chains, facilitating the construction of custom-designed peptides for various biochemical and pharmaceutical applications.