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374229

Sigma-Aldrich

Boc-Tyr-OH

98%

Synonym(s):

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

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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

Quality Level

100

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

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Related Categories

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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

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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
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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
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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
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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
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