6612-79-9 Usage
Description
.beta.-D-Glucopyranose, 1-deoxy-1-(phenyldithio)-, tetraacetate is a chemical compound that features a glucopyranose ring with a phenyl dithioether group attached at the first carbon position, replacing the hydroxyl group. .beta.-D-Glucopyranose, 1-deoxy-1-(phenyldithio)-, tetraacetate is tetraacetylated, which means that each hydroxyl group on the glucose ring is esterified with an acetyl group. .beta.-D-Glucopyranose, 1-deoxy-1-(phenyldithio)-, tetraacetate has potential applications in organic synthesis and can serve as a reagent in chemical reactions to introduce the phenyldithio group to other compounds. It may also be utilized as a building block in the synthesis of more complex organic molecules, with the tetraacetate form being crucial for controlling the reactivity and properties of the compound for specific applications.
Uses
Used in Organic Synthesis:
.beta.-D-Glucopyranose, 1-deoxy-1-(phenyldithio)-, tetraacetate is used as a reagent in organic synthesis for introducing the phenyldithio group to other compounds. This application is valuable for creating a variety of complex organic molecules with specific functional groups.
Used in Chemical Reactions:
.beta.-D-Glucopyranose, 1-deoxy-1-(phenyldithio)-, tetraacetate is used as a building block in the synthesis of more complex organic molecules. Its tetraacetate form is particularly important for controlling the reactivity and properties of the compound, making it suitable for specific applications in chemical reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, .beta.-D-Glucopyranose, 1-deoxy-1-(phenyldithio)-, tetraacetate may be used as a key intermediate in the development of new drugs, particularly those targeting carbohydrate-based interactions or requiring the phenyldithio group for biological activity.
Used in Research and Development:
.beta.-D-Glucopyranose, 1-deoxy-1-(phenyldithio)-, tetraacetate can be employed in research and development settings to study the effects of the phenyldithio group on the chemical and biological properties of various molecules, potentially leading to advancements in the understanding of molecular interactions and the design of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 6612-79-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,1 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6612-79:
(6*6)+(5*6)+(4*1)+(3*2)+(2*7)+(1*9)=99
99 % 10 = 9
So 6612-79-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H24O9S2/c1-11(21)25-10-16-17(26-12(2)22)18(27-13(3)23)19(28-14(4)24)20(29-16)31-30-15-8-6-5-7-9-15/h5-9,16-20H,10H2,1-4H3
6612-79-9Relevant articles and documents
Efficient one-pot synthesis of glycosyl disulfides
Ribeiro Morais, Goreti,Falconer, Robert A.
, p. 7637 - 7641 (2007)
Methodology for the efficient and facile synthesis of glycosyl disulfides is reported. A one-pot procedure employing mild conditions using diethyl azodicarboxylate is described to synthesise a series of glycosyl disulfides in excellent yields.
Novel strategies for the synthesis of unsymmetrical glycosyl disulfides
Morais, Goreti Ribeiro,Springett, Bradley R.,Pauze, Martin,Schr?der, Lisa,Northrop, Matthew,Falconer, Robert A.
, p. 2749 - 2754 (2016/03/05)
Novel strategies for the efficient synthesis of unsymmetrical glycosyl disulfides are reported. Glycosyl disulfides are increasingly important as glycomimetics and molecular probes in glycobiology. Sialosyl disulfides are synthesised directly from the chlorosialoside Neu5Ac2Cl, proceeding via a thiol-disulfide exchange reaction between the sialosyl thiolate and symmetrical disulfides. This methodology was adapted and found to be successfully applicable to the synthesis of unsymmetrical glucosyl disulfides under mild conditions.
Glycosylation via mixed disulfide formation using glycosylthio-phthalimides and -succinimides as glycosylsulfenyl-transfer reagents
Illyés, Tünde-Zita,Szabó, Tamás,Szilágyi, László
, p. 1622 - 1627 (2011/09/14)
The silver salts of tetra-O-acetyl α- or -β-d-glycopyranosyl thiols 1a-4a react smoothly with N-bromophthalimide and N-bromosuccinimide to furnish glycosylthio-phthalimide (1b-4b) and -succinimide (1c-3c) derivatives. Reactions of these reagents with alip
