CAS 93221-21-7
:a-D-Mannopyranosyl isothiocyanate,2,3,4,6-tetraacetate
Description:
α-D-Mannopyranosyl isothiocyanate, 2,3,4,6-tetraacetate is a chemical compound characterized by its structure, which includes a mannopyranosyl moiety linked to an isothiocyanate group and four acetyl groups. This compound is derived from mannose, a six-carbon sugar, and features a pyranose ring, which is a common structural form for sugars. The presence of the isothiocyanate functional group indicates potential biological activity, as isothiocyanates are known for their roles in plant defense mechanisms and have been studied for their anticancer properties. The tetraacetate designation suggests that the hydroxyl groups on the mannopyranosyl unit are acetylated, which can enhance the compound's solubility and stability. This modification may also influence its reactivity and biological interactions. Overall, α-D-Mannopyranosyl isothiocyanate, 2,3,4,6-tetraacetate is of interest in both synthetic chemistry and potential therapeutic applications, particularly in the context of natural product chemistry and medicinal research.
Formula:C15H19NO9S
Synonyms:- 2,3,4,6-Tetra-O-acetyl-伪-D-mannopyranosyl isothiocyanate
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Found 2 products.
2,3,4,6-Tetra-O-acetyl-a-D-mannopyranosyl isothiocyanate
CAS:<p>2,3,4,6-Tetra-O-acetyl-a-D-mannopyranosyl isothiocyanate (TMIT) is a custom synthesis that has been modified to include a fluorine atom. TMIT is a polysaccharide that has been modified by methylation and glycosylation. This compound has been synthesized from the natural carbohydrate D-mannopyranose. TMIT is known for its ability to inhibit protein glycosylation in bacteria cells. It also has high purity with an Oligosaccharide CAS No. 93221-21-7 and modification of saccharides with the addition of methyl groups. The chemical structure of TMIT can be found at 2,3,4,6-Tetra-O-acetyl-a-D-mannopyranosyl isothiocyanate (TMIT).</p>Formula:C15H19NO9SPurity:Min. 95%Molecular weight:389.38 g/mol
