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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:
Molecular Weight:
281.30
Beilstein/REAXYS Number:
2816406
EC Number:
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
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

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related product

Product No.
Description
Pricing

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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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