118464-49-6
Chemical Structure
5-Azido-6-(tert-butyldimethylsilyl)-2,3-O-isopropylidene L-gulono-1,4-lactone
- CAS No.: 118464-49-6
- Formula:C15H27N3O5Si
- Molecular Weight:357.48
IUPAC Name: (3aS,6R,6aS)-6-((R)-1-azido-2-((tert-butyldimethylsilyl)oxy)ethyl)-2,2-dimethyldihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one
InChIKey: DODRPLKUCBFVPS-WYUUTHIRSA-N
SMILES: CC(C)(C)[Si](C)(C)OC[C@H]([C@]1([H])[C@@]2([H])[C@@](OC(C)(O2)C)([H])C(O1)=O)N=[N+]=[N-]
Biological Activity: 5-Azido-6-(tert-butyldimethylsilyl)-2,3-O-isopropylidene L-gulono-1,4-lactone 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].
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5-Azido-6-(tert-butyldimethylsilyl)-2,3-O-isopropylidene L-gulono-1,4-lactone | 5-Azido-6-(tert-butyldimethylsilyl)-2,3-O-isopropylidene L-gulono-1,4-lactone 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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