133697-16-2

4,6-O-Benzylidene-N-(tert-butoxycarbonyl)-1,5-imino-D-glucitol Chemical Structure
133697-16-2

Chemical Structure

4,6-O-Benzylidene-N-(tert-butoxycarbonyl)-1,5-imino-D-glucitol

  • CAS No.: 133697-16-2
  • Formula:C18H25NO6
  • Molecular Weight:351.39

IUPAC Name: tert-butyl (2R,4aR,7S,8R,8aR)-7,8-dihydroxy-2-phenylhexahydro-5H-[1,3]dioxino[5,4-b]pyridine-5-carboxylate

InChIKey: VRFOIPNJKUIHCS-YIDVYQOGSA-N

SMILES: CC(C)(C)OC(N1[C@@]2([H])[C@@]([C@@H]([C@H](C1)O)O)([H])O[C@H](C3=CC=CC=C3)OC2)=O

Biological Activity: 4,6-O-Benzylidene-N-(tert-butoxycarbonyl)-1,5-imino-D-glucitol is 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-W739797
4,6-O-Benzylidene-N-(tert-butoxycarbonyl)-1,5-imino-D-glucitol 4,6-O-Benzylidene-N-(tert-butoxycarbonyl)-1,5-imino-D-glucitol is 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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