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N-Benzyloxycarbonyl-L-alanine, 98%|288428|1142-20-7

N-Benzyloxycarbonyl-L-alanine, 98%

Cat. No JKB11001_5_G
J&K Chemical

Product Information

Product Name
N-Benzyloxycarbonyl-L-alanine, 98%
Brand Name
J&K
Product Number
288428
CAS
1142-20-7
Molecular Formula
C11H13NO4
Molecular Weight
223.23
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
Z-Ala-OH,Carbobenzyloxy-L-alanine
PubChem CID
736104
IUPAC Name
(2S)-2-(phenylmethoxycarbonylamino)propanoic acid
InChI Key
TYRGLVWXHJRKMT-QMMMGPOBSA-N
SMILES
CC@@H(C(=O)O)NC(=O)OCC1=CC=CC=C1

Properties

Melting Point
84-87

References

Generation of Oxyphosphonium Ions by Photoredox/Cobaloxime Catalysis for Scalable Amide and Peptide Synthesis in Batch and Continuous Flow
Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2025
DOI: 10.1007/978-1-0716-4562-8_5

Harnessing the potential of microbial keratinases for bioconversion of keratin waste
Publication Name: Environmental science and pollution research international
Publication Date: 2024-07-10
DOI: 10.1007/s11356-024-34233-6

Remediation of multifarious metal ions and molecular docking assessment for pathogenic microbe disinfection in aqueous solution by waste-derived Ca-MOF
Publication Name: Environmental science and pollution research international
Publication Date: 2024-02-23
DOI: 10.1007/s11356-024-32311-3

A new and promiscuous α/β hydrolase from Acinetobacter tandoii DSM 14970 T inactivates the mycotoxin ochratoxin A
Publication Name: Applied Microbiology and Biotechnology
Publication Date: 2024-02-23
DOI: 10.1007/s00253-024-13073-x

Characterization of thermostable serine hydroxymethyltransferase for β-hydroxy amino acids synthesis
Publication Name: Amino Acids
Publication Date: 2022-12-17
DOI: 10.1007/s00726-022-03205-w

N-Benzyloxycarbonyl-L-alanine, 98%

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