CAS 6884-01-1

α-D-Glucopyranoside, methyl 4,6-O-(phenylmethylene)-, 2,3-bis(4-methylbenzenesulfonate)

Description:

α-D-Glucopyranoside, methyl 4,6-O-(phenylmethylene)-, 2,3-bis(4-methylbenzenesulfonate) is a complex organic compound characterized by its glycosidic structure derived from glucose. This substance features a glucopyranoside moiety, which is a six-membered cyclic form of glucose, modified with phenylmethylene groups at the 4 and 6 positions, enhancing its reactivity and solubility. The presence of two 4-methylbenzenesulfonate groups at the 2 and 3 positions contributes to its sulfonate character, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. This compound is typically used in organic synthesis and may serve as a reagent in carbohydrate chemistry. Its solubility in organic solvents and stability under standard laboratory conditions make it useful for research applications. Additionally, the presence of sulfonate groups can impart unique properties, such as increased polarity and potential for ionic interactions, which can be advantageous in various chemical processes. Overall, this compound exemplifies the intricate modifications that can be made to carbohydrate structures for specialized applications in chemistry.

Formula: C₂₈H₃₀O₁₀S₂

InChI: InChI=1S/C28H30O10S2/c1-18-9-13-21(14-10-18)39(29,30)37-25-24-23(17-34-27(36-24)20-7-5-4-6-8-20)35-28(33-3)26(25)38-40(31,32)22-15-11-19(2)12-16-22/h4-16,23-28H,17H2,1-3H3/t23-,24-,25+,26-,27?,28+/m1/s1

InChI key: InChIKey=MPNMHFPNHIKNOA-GUONBBAESA-N

SMILES: O(S(=O)(=O)C1=CC=C(C)C=C1)[C@H]2[C@]3([C@](O[C@H](OC)[C@@H]2OS(=O)(=O)C4=CC=C(C)C=C4)(COC(O3)C5=CC=CC=C5)[H])[H]

Synonyms:

• 4,6-O-Benzylidene-alpha-D-glucopyranoside methyl bis(4-methylbenzenesulphonate)
• Glucopyranoside, methyl 4,6-O-benzylidene-, di-p-toluenesulfonate, α-<span class="text-smallcaps">D</span>-
• Glucoside, 2,3-ditosyl-4,6-benzylidene-α-methyl-
• Methyl 4,6-O-benzylidene-2,3-di-O-tosyl-α-<span class="text-smallcaps">D</span>-glucopyranoside
• Nsc 89882
• Pyrano[3,2-d]-1,3-dioxin, α-<span class="text-smallcaps">D</span>-glucopyranoside deriv.
• methyl 4,6-O-benzylidene-2,3-bis-O-[(4-methylphenyl)sulfonyl]-alpha-D-glucopyranoside
• methyl 4,6-O-benzylidene-2,3-bis-O-[(4-methylphenyl)sulfonyl]-beta-L-mannopyranoside
• α-<span class="text-smallcaps">D</span>-Glucopyranoside, methyl 4,6-O-(phenylmethylene)-, 2,3-bis(4-methylbenzenesulfonate)
• α-<span class="text-smallcaps">D</span>-Glucopyranoside, methyl 4,6-O-(phenylmethylene)-, bis(4-methylbenzenesulfonate)
• α-D-Glucopyranoside, methyl 4,6-O-(phenylmethylene)-, bis(4-methylbenzenesulfonate)
• Glucopyranoside, methyl 4,6-O-benzylidene-, di-p-toluenesulfonate, α-D-
• α-D-Glucopyranoside, methyl 4,6-O-(phenylmethylene)-, 2,3-bis(4-methylbenzenesulfonate)

Methyl 4,6-O-benzylidene-2,3-di-O-(p-toluenesulfonyl)-α-D-glucopyranoside

CAS: 6884-01-1

Methyl 4,6-O-benzylidene-2,3-di-O-(p-toluenesulfonyl)-a-D-glucopyranoside is a custom synthesis that has been modified with fluorination, methylation, and click modification. It is a monosaccharide that can be found in saccharides and polysaccharides. This product is also a synthetic carbohydrate with the CAS number of 6884-01-1.
Methyl 4,6-O-benzylidene-2,3-di-O-(p-toluenesulfonyl)-a -D -glucopyranoside has been shown to have antihyperglycemic properties by inhibiting the action of alpha amylase on starch. This product also inhibits the activity of alpha amylase on glycogen and lactose.

Formula: C₂₈H₃₀O₁₀S₂

Purity: Min. 95%

Molecular weight: 590.66 g/mol

Ref: 3D-MM70328