CAS 230953-17-0
:β-D-Mannopyranose, O-2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1→3)-O-[2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1→6)]-1,2-O-ethylidene-, acetate
Description:
β-D-Mannopyranose, O-2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1→3)-O-[2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1→6)]-1,2-O-ethylidene-, acetate (CAS 230953-17-0) is a complex carbohydrate derivative characterized by its multiple acetyl groups and specific glycosidic linkages. This compound features a β-D-mannopyranose backbone, which is a six-membered ring sugar, and is heavily acetylated at the hydroxyl groups, enhancing its stability and solubility in organic solvents. The presence of ethylidene and acetate groups suggests that it may exhibit unique reactivity and properties compared to its non-acetylated counterparts. The specific glycosidic linkages (1→3 and 1→6) indicate a branched structure, which can influence its biological activity and interactions with other molecules. Such derivatives are often studied for their potential applications in biochemistry, pharmaceuticals, and as building blocks in glycoscience. Overall, this compound exemplifies the complexity and diversity of carbohydrate chemistry, with implications for both synthetic and natural product chemistry.
Formula:C38H52O25
InChI:InChI=1S/C38H52O25/c1-14(39)48-11-24-27(51-16(3)41)30(54-19(6)44)33(56-21(8)46)36(60-24)50-13-26-29(53-18(5)43)32(35-37(61-26)59-23(10)58-35)63-38-34(57-22(9)47)31(55-20(7)45)28(52-17(4)42)25(62-38)12-49-15(2)40/h23-38H,11-13H2,1-10H3/t23?,24-,25-,26-,27-,28-,29-,30+,31+,32+,33+,34+,35+,36+,37-,38-/m1/s1
InChI key:InChIKey=YWTLKYGRDHOVGY-TXSWQAALSA-N
SMILES:O([C@@H]1[C@]2([C@@](O[C@H](CO[C@@H]3[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O3)[C@H]1OC(C)=O)(OC(C)O2)[H])[H])[C@@H]4[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O4
Synonyms:- β-D-Mannopyranose, O-2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1→3)-O-[2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1→6)]-1,2-O-ethylidene-, acetate
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Found 4 products.
4-O-Acetyl-3,6-di-O-(2,3,4,6-tetra-O-acetyl-a-D-mannopyranosyl)-1,2-ethylidene-b-D-mannopyranose
CAS:Formula:C38H52O25Color and Shape:SolidMolecular weight:908.80454-O-Acetyl-3,6-di-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-1,2-ethylidene-β-D-mannopyranose
CAS:Controlled Product<p>Applications An intermediate for synthesis of bioactive oligosaccharides using 1,2-O-Ethylidene-α-D-gluco- and -β-D-Mannopyranose as the acceptors and acetobromo sugars as the donors via ortho ester intermediates.<br>References Sharp, J., et al.: J. Biol. Chem., 259, 11312 (1984),Cheong, J., et al.: Plant Cell, 3, 137 (1991), Mandal, D., et al.: Biochemistry, 33, 1157 (1994),<br></p>Formula:C38H52O25Color and Shape:NeatMolecular weight:908.84-O-Acetyl-3,6-di-O-(2,3,4,6-tetra-O-acetyl-a-D-mannopyranosyl)-1,2-ethyledine-b-D-mannopyranose
CAS:<p>4-O-Acetyl-3,6-di-O-(2,3,4,6-tetra-O-acetyl-a-D-mannopyranosyl)-1,2-ethyledine (CAS No. 230953-17) is a carbohydrate that has been modified with acetyl groups at the 3 and 6 positions of the monosaccharide unit. This modification is a complex carbohydrate that is made up of oligosaccharides and polysaccharides. The modification causes changes in the chemical properties of the carbohydrate compared to natural saccharides. 4-O-(2,3,4,6) tetra O acetyl a D mannopyranosyl 1 2 ethyledine b D mannopyranose has been used in synthesis of custom sugars for medical applications. It has also shown anti inflammatory activities against Mycobacterium tuberculosis and Mycobacterium avium complex</p>Formula:C38H52O25Purity:Min. 95%Molecular weight:908.8 g/mol
