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Usage

Uses

Used in Pharmaceutical Industry:
2-ACETAMIDO-2-DEOXY-D-GALACTITOL is used as a pharmaceutical compound for its potential therapeutic applications. The expression is: 2-ACETAMIDO-2-DEOXY-D-GALACTITOL is used as a therapeutic agent for its unique chemical properties and potential to interact with biological systems.
Used in Chemical Research:
In the field of chemical research, 2-ACETAMIDO-2-DEOXY-D-GALACTITOL is used as a research compound for studying the effects of the acetamido group substitution on the properties and reactivity of galactitol derivatives. The expression is: 2-ACETAMIDO-2-DEOXY-D-GALACTITOL is used as a research compound for investigating the influence of acetamido group substitution on galactitol derivatives.
Used in Material Science:
2-ACETAMIDO-2-DEOXY-D-GALACTITOL may also find applications in material science, particularly in the development of novel materials with specific properties due to the presence of the acetamido group. The expression is: 2-ACETAMIDO-2-DEOXY-D-GALACTITOL is used as a building block for the development of new materials with unique properties in material science.

InChI:InChI=1/C8H17NO6/c1-4(12)9-5(2-10)7(14)8(15)6(13)3-11/h5-8,10-11,13-15H,2-3H2,1H3,(H,9,12)/t5-,6+,7+,8-/m0/s1

Upstream product

• 72-87-7 N-acetyl-D-galactosamine 
• 5469-77-2 2-Acetamido-2-desoxy-D-galactono-1,4-lacton 
• 1772-03-8 D-(+)-galactosamine hydrochloride 
• 87924-40-1 2-acetamido-2-deoxy-D-galactose N,N'-diphenylformazan 
• 87862-19-9 β-D-GalNAc-(1-4)-β-D-GalNAc-(1-3)-β-D-Gal-(1-4)-β-D-Gal-(1-3)-D-GalNAc-ol 
• 84012-04-4 α-L-Fuc-(1-3)-β-D-GalNAc-(1-3)-β-D-Gal-(1-4)-β-D-Gal-(1-3)-D-GalNAc-ol 
• 72-87-7 N-acetyl-beta-D-galactosamine 
• 134-61-2 N-acetylgalactosamine 

Downstream Products

• 20706-37-0 2-amino-2-deoxy-D-galacticol 
• 56211-19-9 2-acetamido-2-deoxy-D-galacitol pentaacetate 
• 87924-37-6 2-acetamido-2-deoxy-D-galactose phenylhydrazone 
• 87924-45-6 2-acetamido-3,4,5,6-tetra-O-acetyl-2-deoxy-D-galactose N,N'-diphenylformazan 
• 87924-40-1 2-acetamido-2-deoxy-D-galactose N,N'-diphenylformazan 

Relevant academic research and scientific papers

Smith degradation of the O-antigenic polysaccharide of Salmonella Dakar: structural studies of the products

Two different oligosaccharides were obtained from the Smith degradation of the O-polysaccharide isolated from the lipopolysaccharide of Salmonella Dakar. The structures of these oligosaccharides were investigated by chemical analysis, NMR spectroscopy and MALDI-TOF mass spectrometry. The following structures of these products were determined: α-d-GalpNAc-(1→4)-α-d-Quip3NAc-(1→3)-α-l-Rha p-(1→2)-threitol and {A figure is presented}. where Quip3NAc is 3-acetamido-3,6-dideoxyglucose. The reaction products confirmed the structure of the repeating unit of the Salmonella Dakar O-polysaccharide reported previously [Kumirska, J.; Szafranek, J.; Czerwicka, M.; Paszkiewicz, M.; Dziadziuszko, H.; Kunikowska, D.; Stepnowski, P. Carbohydr. Res. 2007, 342, 2138-2143].

2-Acetamido-2-deoxyaldonolactones from sugar formazans

A new approach towards simple aldonic acid derivatives starting from the corresponding aldoses via the 2-acetamido-2-deoxy formazans resulted in the synthesis of 2-acetamido-2-deoxy-D-galactono-1,4-lactone (8), and its 6-deoxy (11) and 6-azido-6-deoxy (14) analogues on treatment with trifluoroacetic acid.The five-membered ring structure of the lactones and that of the intermediate lactone phenylhydrazone (7) was proved by 1H and 13C NMR studies, including deuterium-induced differential isotope shift (DIS) measurements.With sodium borohydride, lactones 8 and 11 were converted into 2-acetamido-2-deoxy-D-galactitol (15) and its 6-deoxy analogue (17), respectively.

UNEXPECTED FORMATION OF 2-ACETAMIDO-2-DEOXY DERIVATIVES OF SUGAR FORMAZANS

A novel method for the preparation of acyclic 2-acetamido-2-deoxy derivatives of sugars was provided by deacetylation of acetylated sugar formazans with ammonia.The stereochemistry of the new 2-acetamido-2-deoxy sugar formazans was established by authenti