Skip to Content
Merck
All Photos(1)

Documents

374229

Sigma-Aldrich

Boc-Tyr-OH

98%

Synonym(s):

N-(tert-Butoxycarbonyl)-L-tyrosine, Boc-L-tyrosine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
4-(HO)C6H4CH2CH(COOH)NHC(O)OC(CH3)3
CAS Number:
3978-80-1
Molecular Weight:
281.30
Beilstein:
2816406
EC Number:
223-613-7
MDL number:
MFCD00037179
UNSPSC Code:
12352209
PubChem Substance ID:
24863291
NACRES:
NA.22

Assay

98%

form

solid

optical activity

[α]20/D +3.0°, c = 2 in acetic acid

reaction suitability

reaction type: Boc solid-phase peptide synthesis

mp

133-135 °C (lit.)

application(s)

peptide synthesis

SMILES string

CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O

InChI

1S/C14H19NO5/c1-14(2,3)20-13(19)15-11(12(17)18)8-9-4-6-10(16)7-5-9/h4-7,11,16H,8H2,1-3H3,(H,15,19)(H,17,18)/t11-/m0/s1

InChI key

CNBUSIJNWNXLQQ-NSHDSACASA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

related product

Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Qi Zhao et al.
Nutrition & metabolism, 15, 57-57 (2018-08-18)
Individuals' peak bone mineral density (BMD) achieved and maintained at ages 20-40 years is the most powerful predictor of low bone mass and osteoporotic fractures later in life. The aim of this study was to identify metabolomic factors associated with peak
M L Da Silva et al.
Archives of biochemistry and biophysics, 312(1), 151-157 (1994-07-01)
The N-linked oligosaccharides from porcine fibrinogen were purified following their release from glycopeptides using N-glycosidase F. In separate experiments, both sialyl and asialyl oligosaccharides were prepared from 5 g of fibrinogen. The reducing oligosaccharides were reacted with ammonium bicarbonate to
Yifan Wang et al.
ACS catalysis, 9(6), 4764-4776 (2019-07-30)
LmbB2 is a peroxygenase-like enzyme that hydroxylates L-tyrosine to L-3,4-dihydroxyphenylalanine (DOPA) in the presence of hydrogen peroxide. However, its heme cofactor is ligated by a proximal histidine, not cysteine. We show that LmbB2 can oxidize L-tyrosine analogs with ring-deactivated substituents
Abe D Pressman et al.
Journal of the American Chemical Society, 141(15), 6213-6223 (2019-03-27)
Molecular evolution can be conceptualized as a walk over a "fitness landscape", or the function of fitness (e.g., catalytic activity) over the space of all possible sequences. Understanding evolution requires knowing the structure of the fitness landscape and identifying the
Esmaeil Salimi et al.
International journal of pharmaceutics, 550(1-2), 200-206 (2018-08-28)
To overcome the mucus layer and cell membrane barrier, self-emulsifying drug delivery systems (SEDDS) exhibiting negative zeta potential, switching to positive values when having reached the cell membrane is a promising approach. Accordingly, a novel conjugate was synthesized by covalent
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service