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β-D-mannopyranosyl-(1->2)-D-mannopyranoside is a disaccharide, which is a type of carbohydrate composed of two monosaccharide units, specifically two D-mannose sugars. The structure of this disaccharide is characterized by a β-D-mannopyranosyl unit linked to another D-mannopyranosyl unit through a glycosidic bond at the 1st carbon of the first sugar and the 2nd carbon of the second sugar. This specific linkage is denoted as (1->2), indicating the positions of the carbon atoms involved in the bond. The compound is significant in biochemistry as it represents a basic building block in the formation of more complex carbohydrates and can be found in various natural products, such as plant cell walls and some glycoproteins. Understanding the structure and properties of such disaccharides is crucial for studying carbohydrate chemistry, enzymatic reactions, and their roles in biological systems.

50271-63-1

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50271-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50271-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,2,7 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 50271-63:
(7*5)+(6*0)+(5*2)+(4*7)+(3*1)+(2*6)+(1*3)=91
91 % 10 = 1
So 50271-63-1 is a valid CAS Registry Number.

50271-63-1Downstream Products

50271-63-1Relevant academic research and scientific papers

Synthesis of |β-(1→2)-linked oligomannosides

Polakova, Monika,Roslund, Mattias U.,Ekholm, Filip S.,Saloranta, Tiina,Leino, Reko

experimental part, p. 870 - 888 (2009/07/17)

β-(1→2)-Linked oligomannosides constitute an important class of carbohydrate structures located on the cell surface of several Candida species, including C. albicans. As a result of the immunostimulating properties of such compounds, the upscaling of their synthesis is relevant. In this paper, a highly stereoselective synthesis of |β-(1→2)-linked oligomannosides was performed by further development of and modifications to the methodologies described earlier in the literature. In addition to the synthesis of fully deprotected β-(1→2)-linked mannobiose and mannotriose, some preliminary modifications to the oligosaccharide core, resulting in close analogues with biological potential, are presented. The fully deprotected products form potential targets for screening against C. albicans and may also result in new model structures for vaccine development.

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