123809-59-6

Basic information

• Product Name: 4-O-(2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl)-D-mannopyranose Tetraacetate
• Synonyms: 4-O-(2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl)-D-mannopyranose Tetraacetate;4-O-(2,3,4,6-Tetra-O-acetyl-a-D-mannopyranosyl)-D-mannopyranose Tetraacetate;2,3,6-Tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-a-D-mannopyranosyl)-D-mannopyranose
• CAS NO: 123809-59-6
• Molecular Formula: C₂₈H₃₈O₁₉
• Molecular Weight: 678.59
• Product Categories: 13C & 2H Sugars;Carbohydrates & Derivatives;Oligosaccharides
• Mol File: 123809-59-6.mol
• Article Data: 1

Chemical Properties

• Melting Point: 59-61°C
• Appearance: /
• Storage Temp.: Hygroscopic, -20°C Freezer, Under Inert Atmosphere
• Solubility: Chloroform, DMSO, Methanol
• CAS DataBase Reference: 4-O-(2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl)-D-mannopyranose Tetraacetate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-O-(2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl)-D-mannopyranose Tetraacetate(123809-59-6)
• EPA Substance Registry System: 4-O-(2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl)-D-mannopyranose Tetraacetate(123809-59-6)

Safety Data

• Hazardous Substances Data: 123809-59-6(Hazardous Substances Data)

Usage

Description

4-O-(2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl)-D-mannopyranose Tetraacetate, with the CAS number 123809-59-6, is a complex organic compound that plays a significant role in the field of organic synthesis. It is characterized by its yellow syrup appearance and possesses unique chemical properties that make it valuable for various applications.

Uses

Used in Organic Synthesis:
4-O-(2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl)-D-mannopyranose Tetraacetate is used as a key intermediate in organic synthesis for the development of various chemical compounds. Its unique structure allows it to be a versatile building block in the synthesis of complex organic molecules, contributing to the advancement of chemical research and the creation of new materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-O-(2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl)-D-mannopyranose Tetraacetate is used as a starting material for the synthesis of drug candidates. Its unique properties enable the development of novel therapeutic agents with potential applications in treating various diseases and medical conditions.
Used in Chemical Research:
4-O-(2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl)-D-mannopyranose Tetraacetate is also utilized in chemical research as a model compound to study the properties and reactions of complex organic molecules. This helps researchers gain a deeper understanding of the underlying chemical processes and mechanisms, ultimately leading to the discovery of new chemical reactions and applications.

Upstream product

• 108-24-7 acetic anhydride 
• 134-96-3 syringic aldehyde 
• 4753-07-5 2,3,6,2',3',4',6'-hepta-O-acetyl-α-D-maltosyl bromide 

Downstream Products

• 4753-07-5 α-hepta-O-acetylmaltosyl bromide 
• 5160-10-1 2,3,6-tetra-O-acetyl-4-O-(2',3',4',6'-tetra-O-acetyl-β-D-galactopyranosyl)-D-glucopyranosylbromide 
• 211676-81-2 Acetic acid (2S,3R,4S,5R,6R)-3-acetoxy-6-acetoxymethyl-2-(3-mercaptomethyl-benzylsulfanyl)-5-((2S,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester 
• 77489-36-2 2,3,6,2',3',4'6'-hepta-O-acetyl-β-D-lactopyranosyl isothiocianate 
• 328408-03-3 2,3,6-tri-O-acetyl-4-O-[2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl]-α-D-glucopyranosyl isothiocyanate 
• 14227-66-8 acetobromocellobiose 
• 495400-10-7 Acetic acid (2R,3R,4S,5R,6R)-3-acetoxy-6-acetoxymethyl-2-(2-hydroxy-5-nitro-benzyloxy)-5-((2S,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester 
• 495400-11-8 Acetic acid (2R,3R,4S,5R,6R)-3-acetoxy-6-acetoxymethyl-2-(5-hydroxy-2-nitro-benzyloxy)-5-((2S,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester 
• 726134-69-6 3-(benzyloxycarbonylamino)propyl (2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-β-D-glucopyranoside 
• 106256-89-7 (2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-β-D-glucopyranosyl trichloroacetimidate 
• 100678-97-5 phenyl (β-D-galactopyranosyl)-(1->4)-β-D-glucopyranoside 
• 847237-46-1 phenyl 4-O-(6-deoxy-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 847237-47-2 (2S,3R,4R,5S,6R)-5-((3aS,4R,6S,7R,7aR)-7-Hydroxy-4-hydroxymethyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-yloxy)-6-hydroxymethyl-2-phenoxy-tetrahydro-pyran-3,4-diol 
• 847237-65-4 phenyl 4-O-(3-O-allyl-β-D-galactopyranosyl)-β-D-glucopyranoside 

Relevant articles and documents

Synthesis of aryl glycosides as vir gene inducers of Agrobacterium tumefaciens

Aryl β-glycopyranosides have been synthesized by coupling syringaldehyde (3-methoxyvanillin) with L-fucose, D-galactose, and maltose; acetosyringone (4-hydroxy-3,5-dimethoxyacetophenone) with L-fucose and maltose; acetovanillone (4-hydroxy-3-methoxyacetophenone) with L-fucose; and syringic acid (4-hydroxy-3,5-dimethoxybenzoic acid) with D-galactose. The procedure using peracetylated glycosyl halides and sodium phenolates in aqueous acetone afforded the acetylated β-glycosides, which were deacetylated. Aryl β-glycopyranosides have been synthesized by coupling syringaldehyde (3-methoxyvanillin) with L-fucose, D-galactose, and maltose; acetosyringone (4-hydroxy-3,5-dimethoxyacetophenone) with L-fucose and maltose; acetovanillone (4-hydroxy-3-methoxyacetophenone) with L-fucose; and syringic acid (4-hydroxy-3,5-dimethoxybenzoic acid) with D-galactose. The procedure using peracetylated glycosyl halides and sodium phenolates in aqueous acetone afforded the acetylated β-glycosides, which were deacetylated.