79414-66-7

Basic information

• Product Name: 1,4,6-TRI-O-ACETYL-2,3-O-CARBONYL-ALPHA-D-MANNOPYRANOSE
• Synonyms: 1,4,6-TRI-O-ACETYL-2,3-O-CARBONYL-ALPHA-D-MANNOPYRANOSE;1,3,6-Tri-O-acetyl-2,4-di-O-benzyl-a-D-glucopyranose;2,4-Di-O-benzyl-1,3,6-tri-O-acetyl-α-D-glucopyranose;2,4-Bis-O-(phenylMethyl)-α-D-glucopyranose Triacetate
• CAS NO: 79414-66-7
• Molecular Formula: C₂₆H₃₀O₉
• Molecular Weight: 486.51
• Product Categories: 13C & 2H Sugars;Carbohydrates & Derivatives
• Mol File: 79414-66-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,4,6-TRI-O-ACETYL-2,3-O-CARBONYL-ALPHA-D-MANNOPYRANOSE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4,6-TRI-O-ACETYL-2,3-O-CARBONYL-ALPHA-D-MANNOPYRANOSE(79414-66-7)
• EPA Substance Registry System: 1,4,6-TRI-O-ACETYL-2,3-O-CARBONYL-ALPHA-D-MANNOPYRANOSE(79414-66-7)

Safety Data

• Hazardous Substances Data: 79414-66-7(Hazardous Substances Data)

Usage

Description

1,4,6-TRI-O-ACETYL-2,3-O-CARBONYL-ALPHA-D-MANNOPYRANOSE is a complex carbohydrate derivative with a unique structure that features acetylated hydroxyl groups and a carbonyl group. 1,4,6-TRI-O-ACETYL-2,3-O-CARBONYL-ALPHA-D-MANNOPYRANOSE is a versatile intermediate in organic synthesis, particularly in the preparation of various biologically active molecules and pharmaceuticals.

Uses

Used in Organic Synthesis:
1,4,6-TRI-O-ACETYL-2,3-O-CARBONYL-ALPHA-D-MANNOPYRANOSE is used as a key intermediate in the synthesis of complex carbohydrate structures and related compounds. Its unique structure allows for selective functionalization and derivatization, making it a valuable building block for the development of novel bioactive molecules and pharmaceutical agents.
Used in Pharmaceutical Industry:
1,4,6-TRI-O-ACETYL-2,3-O-CARBONYL-ALPHA-D-MANNOPYRANOSE is used as a starting material for the synthesis of glycosidic compounds, which are important in the development of new drugs with potential therapeutic applications. 1,4,6-TRI-O-ACETYL-2,3-O-CARBONYL-ALPHA-D-MANNOPYRANOSE's reactivity and structural features enable the creation of diverse glycosidic linkages, which can be crucial for the biological activity and pharmacokinetic properties of the resulting drug candidates.
Used in Research and Development:
1,4,6-TRI-O-ACETYL-2,3-O-CARBONYL-ALPHA-D-MANNOPYRANOSE is utilized in academic and industrial research settings to explore its potential applications in various fields, such as medicinal chemistry, materials science, and biotechnology. Its unique structural features and reactivity make it an attractive target for the development of new synthetic methods and applications.

Upstream product

• 108-24-7 acetic anhydride 
• 61074-17-7 1,6-Anhydro-2,4-di-O-benzyl-β-D-galactopyranose 
• 86861-43-0 3-O-Acetyl-1,6-anhydro-2,4-di-O-benzyl-β-D-mannopyranose 
• 86900-44-9 1,6-anhydro-4-O-benzyl-β-D-mannopyranose 
• 100-39-0 benzyl bromide 
• 86861-42-9 1,6-anhydro-2,4-di-O-benzyl-β-D-mannopyranose 
• 35303-86-7 (2R,3S,4S,5R,6S)-3,5-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-4-ol 
• 3879-79-6 methyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside 
• 97-30-3 methyl-alpha-D-glucopyranoside 

Downstream Products

• 79705-30-9 3,6-di-O-acetyl-2,4-di-O-benzyl-α-D-galactopyranosyl bromide 
• 114283-82-8 Acetic acid (2R,3S,4S,5R)-2-acetoxymethyl-3,5-bis-benzyloxy-6-hydroxy-tetrahydro-pyran-4-yl ester 
• 143826-30-6 N-benzyloxycarbonyl-3-aminopropyl 2,4-di-O-benzyl-β-D-galactopyranoside 
• 143826-31-7 N-benzyloxycarbonyl-3-aminopropyl 2,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-β-D-galactopyranoside 
• 143826-33-9 N-benzyloxycarbonyl-3-aminopropyl 2,4-di-O-benzyl-3-O-levulinoyl-β-D-galactopyranoside 
• 143826-29-3 N-benzyloxycarbonyl-3-aminopropyl 3,6-di-O-acetyl-2,4-di-O-benzyl-β-D-galactopyranoside 
• 143826-32-8 N-benzyloxycarbonyl-3-aminopropyl 2,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-3-O-levulinoyl-β-D-galactopyranoside 
• 79705-38-7 Benzyl-4-O-(3,6-di-O-acetyl-2,4-di-O-benzyl-β-D-galactopyranosyl)-2,3-O-isopropyliden-α-L-rhamnopyranosid 
• 79705-37-6 Benzyl-4-O-(3,6-di-O-acetyl-2,4-di-O-benzyl-α-D-galactopyranosyl)-2,3-O-isopropyliden-α-L-rhamnopyranosid 

Relevant articles and documents

Corrected order in the simultaneous debenzylation-acetolysis of methyl 2,3,4,6-tetra-O-benzyl-α-d-glucopyranoside

The benzyl groups of methyl 2,3,4,6-tetra-O-benzyl-α-d-glucopyranoside were cleaved in the order of 6-O-Bn > 3-O-Bn > 4-O-Bn > 2-O-Bn under acid-mediated conditions in acetic anhydride. The order is a correction of that previously reported.

Synthesis of a pentasaccharide and a heptasaccharide corresponding to an ovarian glycoprotein; studies towards glycosylations

The syntheses of pentasaccharide I and heptasaccharide II, which correspond to an ovarian O-glycoprotein, are presented. The protected pentasaccharide 1 was prepared by condensing a trisaccharide donor (18c) with a disaccharide acceptor (8b), while conden

Building Units of Oligosaccharides, XLVII. - Synthesis of Tri- and Tetrasaccharide Sequences of N-Glycoproteins Including a β-D-Mannosidic Linkage

The trisaccharides α-D-Man-p-(1 -> 6)-β-D-Man-p-(1 -> 4)-D-GlcNAc (37) and α-D-Man-p-(1 -> 3)-β-D-Man-p-(1 -> 4)-D-GlcNAc (43) as well as the key tetrasaccharide α-D-Man-p-(1 -> 3)- 6)>-β-D-Man-p-(1 -> 4)-D-GlcNAc (51), which are parts of th