H-3,4-Dichloro-Phe-OH

Name: H-3,4-Dichloro-Phe-OH | 52794-99-7
Brand: US-CATO
SKU: S57CPTD788082_10_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57CPTD788082_10_MG

Vendor: US-CATO

Product Information

Product Name

H-3,4-Dichloro-Phe-OH

Brand Name

US-CATO

Product Number

CPTD788082

CAS

52794-99-7

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

2761498

IUPAC Name

(2S)-2-amino-3-(3,4-dichlorophenyl)propanoic acid

InChI Key

NRCSJHVDTAAISV-QMMMGPOBSA-N

SMILES

C1=CC(=C(C=C1CC@@H(C(=O)O)N)Cl)Cl

References Data Source From Pubchem

Discovery of non-proteinogenic amino acids inhibiting biofilm formation by S. aureus and methicillin-resistant S. aureus

Publication Name: Bioorganic & Medicinal Chemistry Letters

Publication Date: 2021-09-15

DOI: 10.1016/j.bmcl.2021.128259

Neighbouring group processes in the deamination of protonated phenylalanine derivatives

Publication Name: Organic & Biomolecular Chemistry

Publication Date: 2005-10-21

DOI: 10.1039/b503355a

Characterization of antinociceptive activity of novel endomorphin-2 and morphiceptin analogs modified in the third position

Publication Name: Biochemical Pharmacology

Publication Date: 2005-01-01

DOI: 10.1016/j.bcp.2004.09.011

Structure Elucidation of Peptides with Unnatural Amino Acids Using an Automated Protein Sequencer

Publication Name: Peptides: The Wave of the Future

Publication Date: 2001

DOI: 10.1007/978-94-010-0464-0_136

H-3,4-Dichloro-Phe-OH

Product Information

General Information

References Data Source From Pubchem

Discovery of non-proteinogenic amino acids inhibiting biofilm formation by S. aureus and methicillin-resistant S. aureus

Neighbouring group processes in the deamination of protonated phenylalanine derivatives

Characterization of antinociceptive activity of novel endomorphin-2 and morphiceptin analogs modified in the third position

Structure Elucidation of Peptides with Unnatural Amino Acids Using an Automated Protein Sequencer