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4-Benzoyl-L-phenylalanine, 95%|204322|104504-45-2

4-Benzoyl-L-phenylalanine, 95%

Cat. No JK204322_250_MG
J&K Chemical

Product Information

Product Name
4-Benzoyl-L-phenylalanine, 95%
Brand Name
J&K
Product Number
204322
CAS
104504-45-2
Molecular Formula
C16H15NO3
Molecular Weight
269.30
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
  • (S)-2-Amino-3-(4-benzoylphenyl)propionic acid
  • H-Phe(4-Bz)-OH
PubChem CID
7020128
IUPAC Name
(2S)-2-amino-3-(4-benzoylphenyl)propanoic acid
InChI Key
TVIDEEHSOPHZBR-AWEZNQCLSA-N
SMILES
C1=CC=C(C=C1)C(=O)C2=CC=C(C=C2)CC@@H(C(=O)O)N

Safety Information

Precautionary Statement
P262

References

In situ structure and assembly of the ABC-type tripartite pump MacAB-TolC
Publication Name: Communications Biology
Publication Date: 2025-06-03
DOI: 10.1038/s42003-025-08236-z

Thioether-mediated protein ubiquitination in constructing affinity- and activity-based ubiquitinated protein probes
Publication Name: Nature Protocols
Publication Date: 2025-04-25
DOI: 10.1038/s41596-025-01162-8

An update on thermostable keratinases for protein engineering against feather pollutants
Publication Name: Applied Microbiology and Biotechnology
Publication Date: 2025-03-25
DOI: 10.1007/s00253-025-13459-5

Expanding the Genetic Code in Leishmania tarentolae: A Novel Platform for Membrane Protein Expression with Unnatural Amino Acids
Publication Name: Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology
Publication Date: 2025-03
DOI: 10.1134/s1990747824700399

Probing Antibody Binding Sites on G Protein-Coupled Receptors Using Genetically Encoded Photo-Activatable Cross-Linkers
Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2025
DOI: 10.1007/978-1-0716-4591-8_12

4-Benzoyl-L-phenylalanine, 95%

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