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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 molecules. In β-D-mannopyranosyl-(1->2)-D-mannopyranoside, the D-mannose units are linked together through a glycosidic bond, with the first D-mannose molecule being connected to the second one at the C1 position of the first molecule and the C2 position of the second molecule. This specific arrangement of the glycosidic bond is denoted as β-D-mannopyranosyl-(1->2)-D-mannopyranoside, indicating that the linkage is in a β-configuration and occurs between the first and second carbon atoms. This disaccharide plays a role in various biological processes, including cell recognition and signaling, and is a component of more complex carbohydrates such as polysaccharides and glycoproteins.

50271-58-4

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50271-58-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50271-58-4 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, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50271-58:
(7*5)+(6*0)+(5*2)+(4*7)+(3*1)+(2*5)+(1*8)=94
94 % 10 = 4
So 50271-58-4 is a valid CAS Registry Number.

50271-58-4Downstream Products

50271-58-4Relevant 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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