CAS 5463-33-2

D-Galactose,diethyl dithioacetal

Description:

D-Galactose, diethyl dithioacetal, with the CAS number 5463-33-2, is a chemical compound derived from D-galactose, a monosaccharide sugar. This compound features a dithioacetal functional group, which is characterized by the presence of two sulfur atoms bonded to a carbon atom that is also connected to an alkyl group—in this case, diethyl groups. The presence of the dithioacetal moiety suggests that this compound may exhibit properties typical of thioacetals, such as increased stability under certain conditions and potential reactivity in organic synthesis. D-Galactose itself is known for its role in various biological processes and can be found in dairy products and certain polysaccharides. The diethyl dithioacetal derivative may be utilized in synthetic organic chemistry, particularly in the protection of carbonyl groups or in the synthesis of more complex molecules. As with many organosulfur compounds, it may also exhibit unique physical properties, such as solubility in organic solvents and specific reactivity patterns in chemical reactions.

Formula: C₁₀H₂₂O₅S₂

Synonyms:

• D-Galactose,diethyl mercaptal
• Galactose, diethyl mercaptal, D- (8CI)
• Galactose diethylmercaptal
• Nsc 20706

Diethyl dithioacetal D-galactose

CAS: 5463-33-2

Diethyl dithioacetal D-galactose

Purity: >98%

Molecular weight: 286.41g/mol

Ref: 54-BICL4251

D-Galactose diethyldithioacetal

CAS: 5463-33-2

Ref: 7W-GC0117

D-Galactose diethyldithioacetal

Controlled Product

CAS: 5463-33-2

Formula: C₁₀H₂₂O₅S₂

Color and Shape: Neat

Molecular weight: 286.409

Ref: TR-D209325

D-Galactose diethyldithioacetal

CAS: 5463-33-2

D-Galactose diethyldithioacetal is a phenylhydrazone that has an affinity for the C-3 position of sugars. It is synthesised from D-galactose and diethyldithiocarbonyl chloride, with a borohydride reduction to give the hydroxyl group. The hydroxyl group reacts with methyl glycosides or carbohydrates to produce 3-substituted glycosides or 3-substituted carbohydrate. D-Galactose diethyldithioacetal also inhibits glycosidase enzymes, which are enzymes that break down sugars, and thus prevents the digestion of sugars. The chemical structure of D-galactose diethyldithioacetal was determined by magnetic resonance spectroscopy. The product was found to be L-fucitol (a sweetener) after desulfurization using hydrogen gas for removal of sulfur compounds.

Formula: C₁₀H₂₂O₅S₂

Purity: Min. 95%

Molecular weight: 286.41 g/mol

Ref: 3D-MG00694