90367-90-1

1,2:3,4-Di-O-isopropylidene-6-deoxy-6-nitro-α-D-galactopyranose Chemical Structure
90367-90-1

Chemical Structure

1,2:3,4-Di-O-isopropylidene-6-deoxy-6-nitro-α-D-galactopyranose

  • CAS No.: 90367-90-1
  • Formula:C12H19NO7
  • Molecular Weight:289.28

IUPAC Name: (3aR,5R,5aS,8aS,8bR)-2,2,7,7-tetramethyl-5-(nitromethyl)tetrahydro-5H-bis([1,3]dioxolo)[4,5-b:4',5'-d]pyran

InChIKey: QJFHJCOBVKZJKK-SOYHJAILSA-N

SMILES: [O-][N+](C[C@@H]1[C@@]2([H])[C@@](OC(C)(O2)C)([H])[C@]3([H])[C@](OC(C)(O3)C)([H])O1)=O

Biological Activity: 1,2:3,4-Di-O-isopropylidene-6-deoxy-6-nitro-α-D-galactopyranose 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-W357109
1,2:3,4-Di-O-isopropylidene-6-deoxy-6-nitro-α-D-galactopyranose 1,2:3,4-Di-O-isopropylidene-6-deoxy-6-nitro-α-D-galactopyranose 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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