CAS 85193-95-9
:Methyl 2-(acetylamino)-2-deoxy-4-O-β-<span class="text-smallcaps">D</smallcap>-galactopyranosyl-α-<smallcap>D</span>-glucopyranoside
Description:
Methyl 2-(acetylamino)-2-deoxy-4-O-β-D-galactopyranosyl-α-D-glucopyranoside, with the CAS number 85193-95-9, is a glycoside compound characterized by its structural complexity, featuring both glucopyranoside and galactopyranoside moieties. This compound is typically a white to off-white solid, soluble in polar solvents such as water and methanol, which facilitates its use in various biochemical applications. It possesses functional groups that contribute to its reactivity, including an acetylamino group that can participate in further chemical transformations. The presence of methyl and glycosidic linkages indicates that it may exhibit specific biological activities, potentially acting as a substrate or inhibitor in enzymatic reactions. Its structural features suggest potential applications in medicinal chemistry, particularly in the development of glycosylated compounds for therapeutic purposes. As with many glycosides, it may also exhibit properties related to sweetness or serve as a precursor in the synthesis of more complex carbohydrates. Proper handling and storage conditions are essential to maintain its stability and integrity.
Formula:C15H27NO11
InChI:InChI=1S/C15H27NO11/c1-5(19)16-8-10(21)13(7(4-18)26-14(8)24-2)27-15-12(23)11(22)9(20)6(3-17)25-15/h6-15,17-18,20-23H,3-4H2,1-2H3,(H,16,19)/t6-,7-,8-,9+,10-,11+,12-,13-,14+,15+/m1/s1
InChI key:InChIKey=PKPZITUQXLANSE-ZSCXKYTFSA-N
SMILES:O([C@@H]1[C@@H](CO)O[C@H](OC)[C@H](NC(C)=O)[C@H]1O)[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O
Synonyms:- Methyl 2-(acetylamino)-2-deoxy-4-O-β-D-galactopyranosyl-α-D-glucopyranoside
- α-D-Glucopyranoside, methyl 2-(acetylamino)-2-deoxy-4-O-β-D-galactopyranosyl-
- Methyl a-N-acetyllactosamine
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Found 1 products.
Methyl a-N-acetyllactosamine
CAS:<p>Methyl a-N-acetyllactosamine is a custom synthesis of Methyl a-N-acetylgalactosamine. This compound has been modified by fluorination, methylation, and click modification to yield the desired product. The monosaccharide structure was synthesized from the corresponding glycosyl halide and protected amino acid. The glycosylation reaction between this monosaccharide and the oligosaccharide containing an unprotected hydroxyl group yields the desired product. The purity of this compound is greater than 99%.</p>Formula:C15H27NO11Purity:Min. 95%Molecular weight:397.38 g/mol
