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Merck
CN
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文件

802999

Sigma-Aldrich

2-Acetamido-2-deoxy-β-D-glucopyranosylamine

97% (HPLC)

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别名:
2-Acetamido-1-amino-1,2-dideoxy-β-D-glucopyranose, N-Acetyl-D-glucosylamine
经验公式（希尔记法）:
C8H16N2O5
CAS号:
4229-38-3
分子量:
220.22
MDL编号:
MFCD00057751
UNSPSC代码:
12352116
PubChem化学物质编号:
329768770
NACRES:
NA.22

质量水平

100

检测方案

97% (HPLC)

形式

powder

mp

60 °C

储存温度

2-8°C

SMILES字符串

CC(=O)NC1C(N)OC(CO)C(O)C1O

InChI

1S/C8H16N2O5/c1-3(12)10-5-7(14)6(13)4(2-11)15-8(5)9/h4-8,11,13-14H,2,9H2,1H3,(H,10,12)

InChI key

MCGXOCXFFNKASF-UHFFFAOYSA-N

相关类别

应用

This compound has been used as a building block in a variety of synthetic reactions.

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

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Convergent solid-phase synthesis of N-glycopeptides facilitated by pseudoprolines at consensus-sequence Ser/Thr residues.
Vera Ullmann et al.
Angewandte Chemie (International ed. in English), 51(46), 11566-11570 (2012-09-05)
Ryan Joseph et al.
Organic letters, 15(4), 732-735 (2013-01-26)
Herein is described the chemoselective Cu(II)-HOBt promoted chemical ligation of glycosylamines and peptide thioacids to give N-glycosylated peptides. The method is distinguished from other chemical approaches to peptide N-glycosylation in that (1) it can be employed in the presence of

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