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Merck
CN

374229

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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关于此项目

线性分子式:
4-(HO)C6H4CH2CH(COOH)NHC(O)OC(CH3)3
化学文摘社编号:
分子量:
281.30
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-613-7
Beilstein/REAXYS Number:
2816406
MDL number:
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产品名称

Boc-Tyr-OH, 98%

InChI key

CNBUSIJNWNXLQQ-NSHDSACASA-N

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

SMILES string

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

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

Quality Level

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存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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Abe D Pressman et al.
Journal of the American Chemical Society, 141(15), 6213-6223 (2019-03-27)
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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
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Antiviral research, 153, 1-9 (2018-03-07)
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