跳转至内容
Merck

374229

Sigma-Aldrich

Boc-Tyr-OH

98%

别名:

N-(叔丁氧基羰基-L-酪氨酸, Boc-L-酪氨酸

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About This Item

线性分子式:
4-(HO)C6H4CH2CH(COOH)NHC(O)OC(CH3)3
CAS号:
分子量:
281.30
Beilstein:
2816406
EC號碼:
MDL號碼:
分類程式碼代碼:
12352209
PubChem物質ID:
NACRES:
NA.22

化驗

98%

形狀

solid

光學活性

[α]20/D +3.0°, c = 2 in acetic acid

反應適用性

reaction type: Boc solid-phase peptide synthesis

mp

133-135 °C (lit.)

應用

peptide synthesis

SMILES 字串

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 密鑰

CNBUSIJNWNXLQQ-NSHDSACASA-N

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产品编号
说明
价格

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

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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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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