O-Benzyl-L-tyrosine, 98%

Name: O-Benzyl-L-tyrosine, 98% | 16652-64-5
Brand: J&K Chemical
SKU: JKB12183_5_G
Price: 73.7 USD
Availability: OutOfStock

Cat. No JKB12183_5_G

Vendor: J&K Chemical

Product Information

Product Name

O-Benzyl-L-tyrosine, 98%

Brand Name

J&K

Product Number

205117

CAS

16652-64-5

Molecular Formula

C16H17NO3

Molecular Weight

271.31

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

4-Benzyloxy-L-phenylalanine,L-Tyr(Bzl)-OH

PubChem CID

725701

IUPAC Name

(2S)-2-amino-3-(4-phenylmethoxyphenyl)propanoic acid

InChI Key

KAFHLONDOVSENM-HNNXBMFYSA-N

SMILES

C1=CC=C(C=C1)COC2=CC=C(C=C2)CC@@H(C(=O)O)N

Properties

Melting Point

259

Optical Activity

-10.5 to -8.5 (C=1, AcOH:H2O=(4:1))

Safety Information

Precautionary Statement

P262

References Data Source From Pubchem

Metabolic fingerprinting to elucidate the biodegradation of phosphonoacetic acid and its impact on Penicillium metabolism

Publication Name: Biodegradation

Publication Date: 2025-09-29

DOI: 10.1007/s10532-025-10192-8

An evolved pyrrolysyl-tRNA synthetase with polysubstrate specificity expands the toolbox for engineering enzymes with incorporation of noncanonical amino acids

Publication Name: Bioresources and Bioprocessing

Publication Date: 2023-12-11

DOI: 10.1186/s40643-023-00712-w

Plasticity in ligand recognition at somatostatin receptors

Publication Name: Nature Structural & Molecular Biology

Publication Date: 2022-02-24

DOI: 10.1038/s41594-022-00727-5

Recent advancements in enzyme engineering via site-specific incorporation of unnatural amino acids

Publication Name: World Journal of Microbiology and Biotechnology

Publication Date: 2021-11-06

DOI: 10.1007/s11274-021-03177-1

Protein Building Blocks and the Expansion of the Genetic Code

Publication Name: Synthetic Biology

Publication Date: 2016

DOI: 10.1007/978-3-319-22708-5_4

O-Benzyl-L-tyrosine, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Metabolic fingerprinting to elucidate the biodegradation of phosphonoacetic acid and its impact on Penicillium metabolism

An evolved pyrrolysyl-tRNA synthetase with polysubstrate specificity expands the toolbox for engineering enzymes with incorporation of noncanonical amino acids

Plasticity in ligand recognition at somatostatin receptors

Recent advancements in enzyme engineering via site-specific incorporation of unnatural amino acids

Protein Building Blocks and the Expansion of the Genetic Code