CAS 359437-01-7
:α-D-Glucopyranoside, methyl, tetrakis(hydrogen sulfate), tetrapotassium salt
Description:
α-D-Glucopyranoside, methyl, tetrakis(hydrogen sulfate), tetrapotassium salt is a complex chemical compound characterized by its structure, which includes a glucopyranoside moiety modified with methyl and sulfate groups. This compound is a salt formed from the tetravalent potassium cation and the tetrakis(hydrogen sulfate) anion, indicating the presence of multiple sulfate groups that contribute to its solubility and reactivity in aqueous environments. The glucopyranoside structure suggests that it is a derivative of glucose, which is a common monosaccharide, and the methylation indicates that one of the hydroxyl groups has been replaced with a methyl group, potentially affecting its biological activity and solubility. The presence of multiple sulfate groups enhances its ionic character, making it highly soluble in water and likely influencing its interactions in biological systems. This compound may have applications in biochemical research, particularly in studies involving carbohydrate chemistry or as a reagent in various chemical syntheses.
Formula:C7H14O18S4·4K
InChI:InChI=1S/C7H14O18S4.4K/c1-20-7-6(25-29(17,18)19)5(24-28(14,15)16)4(23-27(11,12)13)3(22-7)2-21-26(8,9)10;;;;/h3-7H,2H2,1H3,(H,8,9,10)(H,11,12,13)(H,14,15,16)(H,17,18,19);;;;/t3-,4-,5+,6-,7+;;;;/m1..../s1
InChI key:InChIKey=KRIXEXCOMPYLQT-RBPNTIJJSA-N
SMILES:O(S(=O)(=O)O)[C@H]1[C@H](OS(=O)(=O)O)[C@@H](COS(=O)(=O)O)O[C@H](OC)[C@@H]1OS(=O)(=O)O.[K]
Synonyms:- α-D-Glucopyranoside, methyl, tetrakis(hydrogen sulfate), tetrapotassium salt
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Found 2 products.
Methyl α-D-Glucopyranoside 2,3,4,6-tetra-O-sulfate, Potassium Salt (Technical Grade)
CAS:Controlled ProductFormula:C7H10O18S4·4KColor and Shape:NeatMolecular weight:666.80Methyl α-D-glucopyranoside 2,3,4,6-tetrasulfate potassium
CAS:<p>Methyl a-D-glucopyranoside 2,3,4,6-tetrasulfate potassium salt is a custom synthesis. It is a modification of a monosaccharide and an oligosaccharide with the use of click chemistry. The product is synthesized by fluorinating the methyl group of the glycosyl hydroxyl group in order to increase its stability. The resulting compound has been shown to have inhibitory effects on bacterial growth and to be effective against methicillin resistant Staphylococcus aureus (MRSA).</p>Formula:C7H14O18S4•K4Purity:Min. 95%Molecular weight:670.83 g/mol
