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Merck
CN

802999

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

97% (HPLC)

别名:

2-Acetamido-1-amino-1,2-dideoxy-β-D-glucopyranose, N-Acetyl-D-glucosylamine

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关于此项目

经验公式(希尔记法):
C8H16N2O5
化学文摘社编号:
分子量:
220.22
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352116
MDL number:
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产品名称

2-Acetamido-2-deoxy-β-D-glucopyranosylamine, 97% (HPLC)

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)

SMILES string

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

InChI key

MCGXOCXFFNKASF-UHFFFAOYSA-N

assay

97% (HPLC)

form

powder

mp

60 °C

storage temp.

2-8°C

Quality Level

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Application

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

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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