49810-41-5

Ethyl 3,4,6-tri-O-acetyl-2-acetamido-2-deoxy-α-D-thioglucopyranoside Chemical Structure
49810-41-5

Chemical Structure

Ethyl 3,4,6-tri-O-acetyl-2-acetamido-2-deoxy-α-D-thioglucopyranoside

  • CAS No.: 49810-41-5
  • Formula:C16H25NO8S
  • Molecular Weight:391.44

IUPAC Name: (2R,3S,4R,5R,6R)-5-acetamido-2-(acetoxymethyl)-6-(ethylthio)tetrahydro-2H-pyran-3,4-diyl diacetate

InChIKey: BHOPGYBLLSFEGH-OXGONZEZSA-N

SMILES: O=C(C)OC[C@H]1O[C@H](SCC)[C@H](NC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O

Biological Activity: Ethyl 3,4,6-tri-O-acetyl-2-acetamido-2-deoxy-α-D-thioglucopyranosideis a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology[1].

Cat. No. Product Name Purity Description Pricing
HY-W302791
Ethyl 3,4,6-tri-O-acetyl-2-acetamido-2-deoxy-α-D-thioglucopyranoside Ethyl 3,4,6-tri-O-acetyl-2-acetamido-2-deoxy-α-D-thioglucopyranosideis a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology.
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