934591-76-1

Usage

Uses

Used in Organic Synthesis:
Methyl (Phenyl 5-Acetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-2-thio-beta-D-glycero-D-galacto-2-nonulopyranosid)onate is used as a chemical reagent in organic synthesis for the preparation of other complex organic molecules. Its unique functional groups allow for versatile reactions and the formation of diverse chemical products.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Methyl (Phenyl 5-Acetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-2-thio-beta-D-glycero-D-galacto-2-nonulopyranosid)onate is used as a precursor for the development of new drugs. Its specific properties and functional groups may contribute to the design and synthesis of pharmaceutical compounds with potential therapeutic applications.
Used in Pharmaceutical Research:
Methyl (Phenyl 5-Acetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-2-thio-beta-D-glycero-D-galacto-2-nonulopyranosid)onate is utilized in pharmaceutical research to explore its potential as a drug candidate. Its unique structure and functional groups may offer new avenues for the treatment of various diseases and conditions, making it a valuable compound for further investigation and development.
Used in Chemical Reactions:
In the realm of chemical reactions, Methyl (Phenyl 5-Acetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-2-thio-beta-D-glycero-D-galacto-2-nonulopyranosid)onate is employed as a reactant to facilitate specific chemical transformations. Its functional groups enable it to participate in a variety of reactions, making it a useful tool for chemists in the synthesis of new compounds and the modification of existing ones.

Upstream product

• 108-24-7 acetic anhydride 
• 7693-46-1 4-Nitrophenyl chloroformate 
• 75-36-5 acetyl chloride 
• 155155-64-9 (4S,5R,6R)-4-Acetoxy-5-acetylamino-2-phenylsulfanyl-6-((1S,2R)-1,2,3-triacetoxy-propyl)-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 118977-25-6 methyl (phenyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-thio-D-glycerol-β-D-galactonon-2-ulopyranoside)onate 

Downstream Products

• 934592-21-9 methyl 5-acetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galactonon-2-ulopyranosylonate-(2->3)-methyl 2,6-di-O-benzyl-β-D-galactopyranoside 
• 934591-89-6 methyl 5-acetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-β-D-galactonon-2-ulopyranosylonate-(2->6)-methyl 2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 934592-18-4 methyl 5-acetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ylopyranosylonate-(2->6)-methyl 2,3,4-tri-O-benzyl-α-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis of an aminooxy derivative of the GM3 antigen and its application in oxime ligation

The anomeric aminooxy GM3 trisaccharide cancer antigen (Neu5Acα2,3Galβ1,4Glcβ-ONH2) has been chemically synthesized using a linear glycosylation approach. The key step involves a highly α(2,3)-stereoselective sialylation to a galactose acceptor

Screening of Neu5Acα(2-6)gal isomer preferences of siglecs with a sialic acid microarray

Sialic acids (Sias) are important terminal sugars on cell surfaces involved in a wide range of protein-carbohydrate interactions. Hence, agents modulating sias-mediated protein interactions are promising inhibitors or vaccine candidates. Here, we report t

O-sialylation with N-acetyl-5-N,4-O-carbonyl-protected thiosialoside donors in dichloromethane: Facile and selective cleavage of the oxazolidinone ring

An N-acetyl-5-N,4-O-carbonyl-protected thiosialoside donor, the structure of which has been defined through X-ray crystallography, was prepared and tested in couplings to a wide range of acceptors. This donor gives excellent yields and α-selectivities in