H-p-Fluoro-DL-Phe-OH

Name: H-p-Fluoro-DL-Phe-OH | 51-65-0
Brand: US-CATO
SKU: S57CPTD787925_10_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57CPTD787925_10_MG

Vendor: US-CATO

Product Information

Product Name

H-p-Fluoro-DL-Phe-OH

Brand Name

US-CATO

Product Number

CPTD787925

CAS

51-65-0

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

4654

IUPAC Name

2-amino-3-(4-fluorophenyl)propanoic acid

InChI Key

XWHHYOYVRVGJJY-UHFFFAOYSA-N

SMILES

C1=CC(=CC=C1CC(C(=O)O)N)F

References Data Source From Pubchem

Plant amino acid analogues as antimicrobial agents

Publication Name: Amino Acids

Publication Date: 2025-10-22

DOI: 10.1007/s00726-025-03484-z

Peptide-Based Drugs: Emerging Treatment Strategies of Lung Cancer by Overcoming Chemoresistance

Publication Name: International Journal of Peptide Research and Therapeutics

Publication Date: 2025-10-01

DOI: 10.1007/s10989-025-10767-2

Engineering of Corynebacterium glutamicum for the synthesis of aromatic compounds

Publication Name: Applied Microbiology and Biotechnology

Publication Date: 2025-05-30

DOI: 10.1007/s00253-025-13520-3

Structural insights into two thiamine diphosphate-dependent enzymes and their synthetic applications in carbon–carbon linkage reactions

Publication Name: Nature Chemistry

Publication Date: 2025-05-14

DOI: 10.1038/s41557-025-01822-y

Leveraging relaxation-optimized 1H–13CF correlations in 4-19F-phenylalanine as atomic beacons for probing structure and dynamics of large proteins

Publication Name: Nature Chemistry

Publication Date: 2025-05-05

DOI: 10.1038/s41557-025-01818-8

H-p-Fluoro-DL-Phe-OH

Product Information

General Information

References Data Source From Pubchem

Plant amino acid analogues as antimicrobial agents

Peptide-Based Drugs: Emerging Treatment Strategies of Lung Cancer by Overcoming Chemoresistance

Engineering of Corynebacterium glutamicum for the synthesis of aromatic compounds

Structural insights into two thiamine diphosphate-dependent enzymes and their synthetic applications in carbon–carbon linkage reactions

Leveraging relaxation-optimized 1H–13CF correlations in 4-19F-phenylalanine as atomic beacons for probing structure and dynamics of large proteins