L-Aspartic acid β-benzyl ester α-t-butyl ester hydrochloride
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L-Aspartic acid β-benzyl ester α-t-butyl ester hydrochloride

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Category
β−Amino Acids
Catalog number
BAT-005858
CAS number
52615-97-1
Molecular Formula
C15H22ClNO4
Molecular Weight
315.79
L-Aspartic acid β-benzyl ester α-t-butyl ester hydrochloride
IUPAC Name
4-O-benzyl 1-O-tert-butyl (2S)-2-aminobutanedioate;hydrochloride
Synonyms
H-Asp(OBzl)-OtBu HCl
InChI
InChI=1S/C15H21NO4.ClH/c1-15(2,3)20-14(18)12(16)9-13(17)19-10-11-7-5-4-6-8-11;/h4-8,12H,9-10,16H2,1-3H3;1H/t12-;/m0./s1
InChI Key
YSDLFDMXCRFHTQ-YDALLXLXSA-N
Canonical SMILES
CC(C)(C)OC(=O)C(CC(=O)OCC1=CC=CC=C1)N.Cl

L-Aspartic acid β-benzyl ester α-t-butyl ester hydrochloride, a chemical compound widely utilized in research and industrial settings, boasts diverse applications.

Pharmaceutical Research: Serving as a crucial intermediate in pharmaceutical synthesis, this compound plays a pivotal role in drug development and production by serving as a precursor to intricate molecules. Researchers harness its potential to craft innovative therapeutic agents with heightened efficacy and reduced adverse effects.

Peptide Synthesis: Central to peptide synthesis, L-Aspartic acid β-benzyl ester α-t-butyl ester hydrochloride acts as a significant reagent with protected functional groups that facilitate the construction of complex peptide chains sans unwanted side reactions. This capability enables the creation of peptides for therapeutic applications, biomolecular exploration, and biochemical assays, propelling advancements in biotechnology.

Chemical Biology: Within the realm of chemical biology, this compound proves invaluable for studying protein-ligand interactions. By incorporating it into peptides or proteins, researchers can probe binding affinities and conformational changes, shedding light on biological pathways and unveiling potential drug targets with intricate precision.

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