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Atomfair Diethyl N-[4-(methylamino)benzoyl]-D-glutamate C17H24N2O5
Description Diethyl N-[4-(methylamino)benzoyl]-D-glutamate (CAS No. 5303-65-1) is a high-purity biochemical reagent with the molecular formula C17H24N2O5. This compound, also known by its IUPAC name diethyl (2R)-2-[[4-(methylamino)benzoyl]amino]pentanedioate , is a specialized derivative of D-glutamate, featuring a 4-(methylamino)benzoyl moiety. It is widely utilized in pharmaceutical research, peptide synthesis, and as a chiral building block in organic chemistry. The product is rigorously tested for purity and stability, ensuring optimal performance in sensitive applications. Available in various quantities, it is supplied with comprehensive analytical data including HPLC, NMR, and MS spectra for quality assurance.
Description
Description
Diethyl N-[4-(methylamino)benzoyl]-D-glutamate (CAS No. 5303-65-1) is a high-purity biochemical reagent with the molecular formula C17H24N2O5. This compound, also known by its IUPAC name diethyl (2R)-2-[[4-(methylamino)benzoyl]amino]pentanedioate, is a specialized derivative of D-glutamate, featuring a 4-(methylamino)benzoyl moiety. It is widely utilized in pharmaceutical research, peptide synthesis, and as a chiral building block in organic chemistry. The product is rigorously tested for purity and stability, ensuring optimal performance in sensitive applications. Available in various quantities, it is supplied with comprehensive analytical data including HPLC, NMR, and MS spectra for quality assurance.
- CAS No: 5303-65-1
- Molecular Formula: C17H24N2O5
- Molecular Weight: 336.4
- Exact Mass: 336.16852187
- Monoisotopic Mass: 336.16852187
- IUPAC Name: diethyl (2R)-2-[[4-(methylamino)benzoyl]amino]pentanedioate
- SMILES: CCOC(=O)CC[C@H](C(=O)OCC)NC(=O)C1=CC=C(C=C1)NC
- Synonyms: diethyl n-[4-(methylamino)benzoyl]-d-glutamate, Diethyl N-(4-(methylamino)benzoyl)-D-glutamate, EINECS 257-481-7, NSC 121190, 1,5-Diethyl N-[4-(methylamino)benzoyl]-D-glutamate
Application
Diethyl N-[4-(methylamino)benzoyl]-D-glutamate is primarily used as an intermediate in the synthesis of bioactive peptides and pharmaceutical compounds. Its chiral structure makes it valuable for asymmetric synthesis and drug development, particularly in targeting neurological and metabolic pathways. Researchers also employ it in proteomics studies and as a precursor for modified amino acid derivatives. The compound’s stability and reactivity under mild conditions make it suitable for controlled coupling reactions in solid-phase peptide synthesis (SPPS).
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