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O-tert-Butyl-L-tyrosine, 97%|198721|18822-59-8

O-tert-Butyl-L-tyrosine, 97%

Cat. No JKB12187_5_G
J&K Chemical

Product Information

Product Name
O-tert-Butyl-L-tyrosine, 97%
Brand Name
J&K
Product Number
198721
CAS
18822-59-8
Molecular Formula
C13H19NO3
Molecular Weight
237.29
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
H-Tyr(tBu)-OH
PubChem CID
7408092
IUPAC Name
(2S)-2-amino-3-4-(2-methylpropan-2-yl)oxyphenylpropanoic acid
InChI Key
SNZIFNXFAFKRKT-NSHDSACASA-N
SMILES
CC(C)(C)OC1=CC=C(C=C1)CC@@H(C(=O)O)N

Properties

Melting Point
238-243
Optical Activity
-9.0 to -4.0 (C=1, 1 M HCl)

Safety Information

Precautionary Statement
P262

References Data Source From Pubchem

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

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

Incorporation of Azide and Alkyne Functionalities into Peptides
Publication Name: Science of Synthesis
Publication Date: 2021

Expanding the enzyme universe with genetically encoded unnatural amino acids
Publication Name: Nature Catalysis
Publication Date: 2020-01-06
DOI: 10.1038/s41929-019-0410-8

Deaminative Bromination (Bromodediazoniation) of Chiral α-Amino Acids
Publication Name: Science of Synthesis
Publication Date: 2007

O-tert-Butyl-L-tyrosine, 97%

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