13639-58-2

Usage

Uses

Used in Organic Chemistry Research:
2,3,4-tri-O-acetyl-1-S-carbamimidoyl-1-thiopentopyranose is used as a research compound for studying its unique structural properties and reactivity. Its synthesis and study are of interest to scientists working in the fields of carbohydrate chemistry, pharmaceuticals, and bioorganic chemistry.
Used in Pharmaceutical Industry:
2,3,4-tri-O-acetyl-1-S-carbamimidoyl-1-thiopentopyranose is used as a potential building block for the development of new drugs. Its unique structural properties and reactivity make it a valuable component in the design and synthesis of novel pharmaceutical compounds.
Used in Material Science:
2,3,4-tri-O-acetyl-1-S-carbamimidoyl-1-thiopentopyranose is used as a potential component in the development of new materials. Its unique structural properties and reactivity can contribute to the creation of innovative materials with specific properties and applications in various industries.

Upstream product

• 17356-08-0 thiourea 
• 3068-29-9 2,3,4-tri-O-acetyl-β-D-arabinosyl bromide 
• 3068-31-3 1-bromo-2,3,4-tri-O-acetyl-α-D-xylopyranose 
• 3068-31-3 2,3,4-tri-O-acetyl-α-D-xylopyranosyl bromide 

Relevant academic research and scientific papers

S -Glycosides: Synthesis of S -linked arabinoxylan oligosaccharides

S-Glycosides are important tools for the elucidation of specific protein-carbohydrate interactions and can significantly aid structural and functional studies of carbohydrate-active enzymes, as they are often inert or act as enzyme inhibitors. In this con

Synthesis of novel thioglycoside derivatives containing quinazolinone

Aseries of novel thioglycoside derivatives containing 4(3H)-quinazolinone was designed and synthesized from 2-chloromethyl-quinazolin-4(3H)-ones and 1-thioglycose. Several 2-chloromethyl-quinazolin-4(3H)-ones were synthesized on refluxing with 2-(chloroacetylamino)-benzoic acid and arylamines in acetonitrile. All of the novel compounds were characterized by IR, 1H NMR spectra and elemental analysis. The structures of compounds 7b, 8b and 8c have been determined by X-ray diffraction analysis.

Stereoselective synthesis of thioxylooligosaccharides from S-glycosyl isothiourea precursors

A stereoselective synthesis of thioxylo-di-, -tri-, -tetra- and -penta-saccharides from S-glycosyl isothiourea precursors is described. The synthesis was performed starting from 2,3,4-tri-O-acetyl-β-D-xylopyranosyl isothiouronium bromide using a triethylamine promoted reaction with 1,2,3-tri-O-benzoyl-4-O-trifluoromethanesulphonyl-β-L-arabinopyranose. The resulting 4-thioxylobiose was then converted into the corresponding isothiouronium bromide and used for the synthesis of 4,4′-dithioxylotriose. Higher homologues of the series and their α-methyl glycosides were also prepared.