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Merck
CN

15131

Sigma-Aldrich

Boc-Lys(Boc)-OSu

≥97.0% (calc. based on dry substance, C/N)

别名:

Nα,Nε-二叔丁氧羰基-L-赖氨酸 N-丁二酰亚胺酯

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About This Item

经验公式(希尔记法):
C20H33N3O8
CAS号:
分子量:
443.49
Beilstein:
1559007
MDL编号:
UNSPSC代码:
12352202
eCl@ss:
32160406
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

≥97.0% (calc. based on dry substance, C/N)

旋光性

[α]20/D −25.5±1.5°, c = 1% in DMF

反应适用性

reaction type: Boc solid-phase peptide synthesis

应用

peptide synthesis

储存温度

−20°C

SMILES字符串

CC(C)(C)OC(=O)NCCCC[C@H](NC(=O)OC(C)(C)C)C(=O)ON1C(=O)CCC1=O

InChI

1S/C20H33N3O8/c1-19(2,3)29-17(27)21-12-8-7-9-13(22-18(28)30-20(4,5)6)16(26)31-23-14(24)10-11-15(23)25/h13H,7-12H2,1-6H3,(H,21,27)(H,22,28)/t13-/m0/s1

InChI key

IQVLXQGNLCPZCL-ZDUSSCGKSA-N

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WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Haopeng Xiao et al.
Nature communications, 9(1), 1692-1692 (2018-04-29)
Protein glycosylation is ubiquitous in biological systems and essential for cell survival. However, the heterogeneity of glycans and the low abundance of many glycoproteins complicate their global analysis. Chemical methods based on reversible covalent interactions between boronic acid and glycans

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