Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

802999

Sigma-Aldrich

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

97% (HPLC)

Synonym(s):

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

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C8H16N2O5
CAS Number:
4229-38-3
Molecular Weight:
220.22
MDL number:
MFCD00057751
UNSPSC Code:
12352116
PubChem Substance ID:
329768770
NACRES:
NA.22

Quality Level

100

Assay

97% (HPLC)

form

powder

mp

60 °C

storage temp.

2-8°C

SMILES string

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service