CAS 29776-43-0
:2-acetamido-4,6-O-benzylidene-2-deoxy-*D-glucopyr
Description:
2-Acetamido-4,6-O-benzylidene-2-deoxy-D-glucopyranose, with the CAS number 29776-43-0, is a carbohydrate derivative that exhibits several notable characteristics. This compound features a glucopyranose backbone, which is a six-membered ring structure typical of many sugars. The presence of an acetamido group indicates that it has an amide functional group, contributing to its solubility and reactivity. The benzylidene moiety suggests that it has a phenyl group attached through a double bond to an oxygen atom, which can influence its chemical stability and interactions. This compound is typically used in biochemical research and synthesis due to its potential applications in glycoscience and medicinal chemistry. Its structural modifications can affect its biological activity, making it a subject of interest for studies related to enzyme interactions and carbohydrate recognition. Overall, the unique combination of functional groups in this molecule allows for diverse chemical behavior and potential applications in various fields of chemistry and biochemistry.
Formula:C15H19NO6
InChI:InChI=1/C15H19NO6/c1-8(17)16-11-12(18)13-10(21-14(11)19)7-20-15(22-13)9-5-3-2-4-6-9/h2-6,10-15,18-19H,7H2,1H3,(H,16,17)/t10-,11-,12-,13-,14?,15?/m1/s1
SMILES:CC(=N[C@@H]1[C@H]([C@H]2[C@@H](COC(c3ccccc3)O2)OC1O)O)O
Synonyms:- 2-Acetamido-4,6-O-benzylidene-2-deoxy-D-glucopyranose
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Found 5 products.
2-Acetamido-4,6-o-benzylidene-2-deoxy-D-glucopyranose
CAS:<p>2-Acetamido-4,6-o-benzylidene-2-deoxy-D-glucopyranose</p>Purity:≥95%Color and Shape:SolidMolecular weight:309.31g/molN-((4aR,7R,8R,8aS)-6,8-Dihydroxy-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-yl)acetamide
CAS:Purity:95.0%Molecular weight:309.31799316406252-Acetamido-4,6-O-benzylidene-2-deoxy-D-glucopyranose
CAS:<p>2-Acetamido-4,6-O-benzylidene-2-deoxy-D-glucopyranose is an ether of d-glucosamine. It is formed by the reaction of benzyl alcohol and acetamidine with sodium methoxide in the presence of a catalyst. The stereoselectivity of this reaction can be tuned by using different alkali metals as catalysts. The nature and reactivity of the metal cation determines whether 2-acetamido-4,6-O-benzylidene-2,3,5,6,-tetraacetate or 2,3,5,6,-tetraacetate will be produced.</p>Formula:C15H19NO6Purity:Min. 95%Color and Shape:White PowderMolecular weight:309.31 g/mol2-Acetamido-4,6-O-benzylidene-2-deoxy-D-glucopyranose
CAS:Controlled ProductFormula:C15H19NO6Color and Shape:NeatMolecular weight:309.31




