CAS 28140-37-6
:1,2-O-(1-ethoxyethylidene)-beta-D-manno-pyranose
Description:
1,2-O-(1-ethoxyethylidene)-beta-D-manno-pyranose is a glycoside derivative of D-mannose, characterized by the presence of an ethoxyethylidene group at the anomeric position. This compound typically exhibits a pyranose ring structure, which is a six-membered cyclic form of sugars. The presence of the ethoxyethylidene group influences its solubility and reactivity, making it more hydrophobic compared to its parent sugar. This modification can also affect its biological activity, potentially enhancing its stability against enzymatic hydrolysis. The compound is likely to participate in various chemical reactions typical of sugars, such as oxidation, reduction, and glycosylation. Its applications may extend to fields such as biochemistry and pharmaceuticals, where it could serve as a building block for more complex molecules or as a potential therapeutic agent. As with many sugar derivatives, it may also exhibit specific interactions with biological macromolecules, influencing its utility in research and development.
Formula:C16H24O10
InChI:InChI=1/C16H24O10/c1-6-21-16(5)25-14-13(23-10(4)19)12(22-9(3)18)11(7-20-8(2)17)24-15(14)26-16/h11-15H,6-7H2,1-5H3
SMILES:CCOC1(C)OC2C(C(C(COC(=O)C)OC2O1)OC(=O)C)OC(=O)C
Synonyms:- 1,2-O-(1-Ethoxyethylidene)-beta-D-mannopyranose triacetate
- 3,4,6-tri-O-acetyl-1,2-O-(1-ethoxyethylidene)hexopyranose
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Found 3 products.
3,4,6-Tri-O-acetyl-1,2-O-(1-ethoxyethylidene)-β-D-mannopyranose
CAS:<p>3,4,6-Tri-O-acetyl-1,2-O-(1-ethoxyethylidene)-β-D-mannopyranose</p>Purity:>98%Color and Shape:SolidMolecular weight:376.36g/mol3,4,6-Tri-O-acetyl-1,2-O-ethoxyethylidene-β-D-mannopyranose
CAS:<p>3,4,6-Tri-O-acetyl-1,2-O-ethoxyethylidene-b-D-mannopyranose is a synthetic monosaccharide that is used as a substrate for the production of various oligosaccharides and polysaccharides. This substance can be fluorinated to produce 3,4,6-tri-O-(3′,5′ -difluoro) acetyl-1,2:5′,6′ -di(O—ethoxyethylidene)-b-D mannopyranose. It has been shown that methylation of the C1 position in this compound results in a variety of different compounds with different properties. In addition to its use as a substrate in organic synthesis, 3,4,6 triacetyl 1,2:5', 6'-di(O—ethoxyethylidene)-b D mannopyranose is also</p>Formula:C16H24O10Purity:Min. 95%Molecular weight:376.36 g/mol


