5-tert-Butyl N-Benzyloxycarbonyl-L-glutamate TCI C1715

Chemical Identity

Other names: Z-Glu(OtBu)-OH · N-Carbobenzoxy-L-glutamic Acid 5-tert-Butyl Ester · 5-tert-Butyl N-Cbz-L-glutamate · N-Cbz-L-glutamic Acid 5-tert-Butyl Ester · Z-Glu(OtBu)-OH · 5-tert-Butyl N-Carbobenzoxy-L-glutamate · N-Benzyloxycarbony
CAS No.: 3886-08-6
PubChem: CID 107472·SID 87566688
Formula: C17H23NO6
Molecular weight: 337.37 g/mol
Purity: >98.0%(HPLC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-5-[(2-methylpropan-2-yl)oxy]-5-oxo-2-(phenylmethoxycarbonylamino)pentanoic acid
SMILES: CC(C)(C)OC(=O)CCC(C(=O)O)NC(=O)OCC1=CC=CC=C1
InChIKey: GLMODRZPPBZPPB-ZDUSSCGKSA-N
MDL: MDL00038274

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TCI C1715 3886-08-6 5-tert-Butyl N-Benzyloxycarbonyl-L-glutamate is a chemical compound widely used in laboratory settings for peptide synthesis and chemical biology research. This compound is known for its ability to participate in various chemical reactions, especially in the modification of molecules and the development of new pharmaceutical compounds. Its structural complexity and reactivity make it a valuable tool in both academic and industrial research. The compound is available in a solid form and is soluble in organic solvents, making it suitable for a wide range of experimental applications. Due to its stability under controlled conditions, it is commonly used in laboratories across Indonesia for advanced chemical and biochemical studies. Its versatility and reliability in chemical reactions have made it a preferred choice for researchers working in the fields of pharmacology and biotechnology.

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Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 18

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KEMPNY et al. (1995). ChemInform Abstract: A Simple Preparation of Mono‐tert‐butyl Benzyloxycarbonyl‐L‐glutamates.. ChemInform doi:10.1002/chin.199544217
Liu (2011). tert-Butyl Nitrite. Synlett doi:10.1055/s-0030-1259948
Kempny et al. (1995). A SIMPLE PREPARATION OF MONO-tert-BUTYL BENZYLOXYCARBONYL-L-GLUTAMATES. Organic Preparations and Procedures International doi:10.1080/00304949509458473

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.