N-α-Carbobenzoxy-L-glutamic acid γ-cyclohexyl ester
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N-α-Carbobenzoxy-L-glutamic acid γ-cyclohexyl ester

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Category
CBZ-Amino Acids
Catalog number
BAT-001440
CAS number
111479-42-6
Molecular Formula
C19H25NO6
Molecular Weight
363.41
IUPAC Name
5-cyclohexyloxy-5-oxo-2-(phenylmethoxycarbonylamino)pentanoic acid
Synonyms
Z-Glu(OcHex)-OH
InChI
InChI=1S/C19H25NO6/c21-17(26-15-9-5-2-6-10-15)12-11-16(18(22)23)20-19(24)25-13-14-7-3-1-4-8-14/h1,3-4,7-8,15-16H,2,5-6,9-13H2,(H,20,24)(H,22,23)
InChI Key
ZSBFBHHGGYFEAH-UHFFFAOYSA-N
Canonical SMILES
C1CCC(CC1)OC(=O)CCC(C(=O)O)NC(=O)OCC2=CC=CC=C2

N-α-Carbobenzoxy-L-glutamic acid γ-cyclohexyl ester is a chemical compound with diverse applications in peptide synthesis and pharmaceutical research.

Peptide Synthesis: Serving as a protective shield for the amino group during peptide synthesis, N-α-Carbobenzoxy-L-glutamic acid γ-cyclohexyl ester plays a pivotal role in minimizing undesired side reactions. Its exceptional stability and ease of removal make it a preferred choice for producing peptides of exceptional purity, elevating the standards of peptide chemistry.

Pharmaceutical Research: In the realm of drug discovery, this compound acts as a crucial intermediate for synthesizing various pharmaceutical agents. It empowers researchers to construct intricate molecular frameworks essential for drug candidate development. Leveraging this ester enables fine-tuning of pharmacological characteristics at the molecular level, driving advancements in drug design and efficacy optimization.

Material Science: N-α-Carbobenzoxy-L-glutamic acid γ-cyclohexyl ester contributes to the creation of cutting-edge polymeric materials. Its unique structural attributes facilitate the integration of specialized functionalities into polymers, enhancing their mechanical and chemical properties. This breakthrough fosters progress in material science, ushering in advancements in biomedical applications like drug delivery systems and tissue engineering constructs.

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