Nom du produit:1,3,4,6-Tetra-O-acetyl-beta-d-mannopyranose

IUPAC Name:[(2R,3R,4R,5S,6S)-3,4,6-tris(acetyloxy)-5-hydroxyoxan-2-yl]methyl acetate

CAS:18968-05-3
Formule moléculaire:C14H20O10
Pureté:97%
Numéro de catalogue:CM100814
Poids moléculaire:348.3

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Détails du produit

N° CAS:18968-05-3
Formule moléculaire:C14H20O10
Point de fusion:-
Code SMILES:O[C@@H]1[C@H](OC(C)=O)O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Densité:1.757 g/cm3
Numéro de catalogue:CM100814
Poids moléculaire:348.3
Point d'ébullition:425.537°C at 760 mmHg
N° Mdl:MFCD00012354
Stockage:Store at 2-8°C.

Category Infos

Mannose Derivatives
Mannose is a sugar monomer of the aldohexose series of carbohydrates. It is a C-2 epimer of glucose. Mannose is important in human metabolism, especially in the glycosylation of certain proteins.

Column Infos

Carbohydrates
Carbohydrates are polyhydroxy aldehydes (aldoses) or polyhydroxy ketones (ketoses) composed of C, H and O, or form polyhydroxy aldehydes or ketones upon hydrolysis. Carbohydrates come in the form of monosaccharides, disaccharides, oligosaccharides and polysaccharides. The simplest sugars, monosaccharides and disaccharides, consist of one or two monosaccharide units. Oligosaccharides are generally classified as carbohydrates containing 3-10 monosaccharide units. Polysaccharides contain more than 10 monosaccharide units and can be quite large. Glucose is an aldose, the most important monosaccharide in the body, used by cells as fuel. Other aldohexoses are galactose and mannose, which form part of complex molecules. Fructose is a ketohexose sugar, while ribose is the most important aldose pentose sugar and a component of RNA.


Product Other Information

Product Overview 1,3,4,6-Tetra-O-acetyl-beta-d-mannopyranose, otherwise known as TA-4-M, is a sugar derivative found in many plants and fungi, including mushrooms, and is used in the synthesis of various compounds. TA-4-M is a highly polar molecule and has been the subject of much scientific research in recent years.
Synthesis and Application TA-4-M is synthesized through a two-step process involving the acylation of mannose and the acetylation of the resulting intermediate. In the first step, mannose is reacted with an acylating agent, such as an alkyl halide, in the presence of a base, such as sodium hydroxide. The reaction yields the intermediate, 1,3,4,6-tetra-O-acyl-beta-d-mannopyranose. In the second step, the intermediate is reacted with acetic anhydride in the presence of a base, such as sodium hydroxide, to yield TA-4-M. TA-4-M has been used in a variety of scientific research applications, including drug delivery, gene therapy, and cancer research. In drug delivery, TA-4-M is used to transport drugs to specific tissues and organs, allowing for more efficient drug delivery and improved efficacy. In gene therapy, TA-4-M is used to deliver genes to cells, allowing for the introduction of new genetic material into cells. In cancer research, TA-4-M is used to deliver drugs to tumor cells, allowing for more targeted treatment of cancer.
Future Directions The future of TA-4-M in scientific research is promising. One potential future direction is the development of new synthesis methods that allow for the production of TA-4-M in larger quantities and at lower costs. Another potential future direction is the development of new applications for TA-4-M, such as the use of TA-4-M in drug delivery systems and gene therapy. Additionally, further research into the biochemical and physiological effects of TA-4-M could lead to new and improved treatments for a variety of diseases.