DL-Glutamic acid γ-tert-butyl ester
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DL-Glutamic acid γ-tert-butyl ester

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Category
DL-Amino Acids
Catalog number
BAT-001643
CAS number
2241393-62-2
Molecular Formula
C9H17NO4
Molecular Weight
203.20
IUPAC Name
2-amino-5-[(2-methylpropan-2-yl)oxy]-5-oxopentanoic acid
Synonyms
DL-Glu(OtBu)-OH; DL-Glutamic acid 5-tert-butyl ester; 2-amino-5-(tert-butoxy)-5-oxopentanoic acid
Density
1.1±0.1 g/cm3
Boiling Point
336.4±37.0 °C at 760 mmHg
Storage
Store at 2-8 °C
InChI
InChI=1S/C9H17NO4/c1-9(2,3)14-7(11)5-4-6(10)8(12)13/h6H,4-5,10H2,1-3H3,(H,12,13)
InChI Key
OIOAKXPMBIZAHL-UHFFFAOYSA-N
Canonical SMILES
CC(C)(C)OC(=O)CCC(C(=O)O)N

DL-Glutamic acid γ-tert-butyl ester, a versatile chemical compound, finds wide-ranging applications in pharmaceutical research and chemical synthesis.

Pharmaceutical Synthesis: Serving as a pivotal intermediate in pharmaceutical and peptide drug synthesis, DL-Glutamic acid γ-tert-butyl ester plays a crucial role. Its stability and reactivity attributes render it a valuable building block for constructing intricate molecules. This compound expedites the drug development process by aiding in the generation of novel therapeutic agents, thus fostering innovation in pharmaceutical science.

Peptide Modification: Within the realm of peptide chemistry, DL-Glutamic acid γ-tert-butyl ester emerges as a key player in introducing protective groups during synthesis. This functionality facilitates the targeted modification of amino acids, empowering researchers to finely tune peptide chains with precision. Such precision is essential for creating modified peptides endowed with heightened stability and bioactivity, essential for therapeutic applications.

Biotechnology Research: In the domain of biotechnology, DL-Glutamic acid γ-tert-butyl ester is a vital tool for delving into amino acid transport and metabolism. Researchers harness this compound to explore the significance of glutamic acid derivatives in cellular processes, unraveling intricate mechanisms that underpin metabolic pathways.

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