247027-79-8

Basic information

• Product Name: 4-METHOXYPHENYL 2,4,6-TRI-O-BENZYL-BETA-D-GALACTOPYRANOSIDE
• Synonyms: 4-METHOXYPHENYL 2,4,6-TRI-O-BENZYL-BETA-D-GALACTOPYRANOSIDE;4-Methoxyphenyl2,4,6-tri-O-benzyl-b-D-galactopyranoside;4-Methoxyphenyl 2,4,6-Tri-O-benzyl-β-D-galactopyranoside;4-Methoxyphenyl 2,4,6-tri-O-benzyl-β-D-galactopyranoside ,98%;4-Methoxyphenyl 2,4,6-Tri-O-benzyl-β(2R,3R,4S,5R,6S)-3,5-Bis(benzyloxy)-2-((benzyloxy)methyl)-6-(4-methoxyphenoxy)tetrahydro-2H-pyran-4-ol
• CAS NO: 247027-79-8
• Molecular Formula: C₃₄H₃₆O₇
• Molecular Weight: 556.65
• Product Categories: Biochemistry;Galactose;Glycosides;Sugars
• Mol File: 247027-79-8.mol
• Article Data: 4

Chemical Properties

• Melting Point: 94 °C
• Boiling Point: 705.094oC at 760 mmHg
• Flash Point: 380.227oC
• Appearance: /
• Density: 1.243g/cm3
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: -14.5 ° (C=1, CHCl3)
• Storage Temp.: Freezer
• Solubility: slightly sol. in Chloroform
• PKA: 12.71±0.70(Predicted)
• CAS DataBase Reference: 4-METHOXYPHENYL 2,4,6-TRI-O-BENZYL-BETA-D-GALACTOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHOXYPHENYL 2,4,6-TRI-O-BENZYL-BETA-D-GALACTOPYRANOSIDE(247027-79-8)
• EPA Substance Registry System: 4-METHOXYPHENYL 2,4,6-TRI-O-BENZYL-BETA-D-GALACTOPYRANOSIDE(247027-79-8)

Safety Data

• Hazardous Substances Data: 247027-79-8(Hazardous Substances Data)

Usage

Description

4-METHOXYPHENYL 2,4,6-TRI-O-BENZYL-BETA-D-GALACTOPYRANOSIDE is a white powder chemical compound that serves as a key intermediate in the synthesis of various complex carbohydrates and glycoconjugates. It is particularly useful in the preparation of C-glycoside analogues and hexasaccharide, which is a repeating unit found in the cell wall lipopolysaccharide of Azospirillum lipoferum Sp59b.

Uses

Used in Carbohydrate Chemistry:
4-METHOXYPHENYL 2,4,6-TRI-O-BENZYL-BETA-D-GALACTOPYRANOSIDE is used as a synthetic intermediate for the preparation of C-glycoside analogues and hexasaccharide. This is due to its ability to serve as a building block for more complex carbohydrate structures, which are essential in various biological processes and have potential applications in pharmaceuticals and biochemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-METHOXYPHENYL 2,4,6-TRI-O-BENZYL-BETA-D-GALACTOPYRANOSIDE is used as a key component in the development of novel drug candidates targeting various diseases. Its role in synthesizing complex carbohydrates and glycoconjugates makes it a valuable asset in the creation of new therapeutic agents.
Used in Biochemical Research:
4-METHOXYPHENYL 2,4,6-TRI-O-BENZYL-BETA-D-GALACTOPYRANOSIDE is also utilized in biochemical research as a tool to study the structure and function of carbohydrates and their interactions with proteins and other biomolecules. This knowledge can be applied to better understand the role of carbohydrates in cellular processes and the development of new diagnostic and therapeutic strategies.
Used in Material Science:
In the field of material science, 4-METHOXYPHENYL 2,4,6-TRI-O-BENZYL-BETA-D-GALACTOPYRANOSIDE can be used to develop new materials with unique properties, such as improved biocompatibility or enhanced interaction with biological systems. This can lead to the creation of advanced materials for use in medical devices, drug delivery systems, and other applications.
Overall, 4-METHOXYPHENYL 2,4,6-TRI-O-BENZYL-BETA-D-GALACTOPYRANOSIDE is a versatile compound with a wide range of applications across various industries, including pharmaceuticals, biochemistry, and material science. Its ability to serve as a synthetic intermediate for complex carbohydrates and glycoconjugates makes it a valuable asset in the development of new drugs, diagnostic tools, and advanced materials.

InChI:InChI=1/C34H36O7/c1-36-28-17-19-29(20-18-28)40-34-33(39-23-27-15-9-4-10-16-27)31(35)32(38-22-26-13-7-3-8-14-26)30(41-34)24-37-21-25-11-5-2-6-12-25/h2-20,30-35H,21-24H2,1H3/t30-,31+,32+,33-,34-/m1/s1

Upstream product

• 247027-78-7 p-methoxyphenyl 3-O-allyl-2,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 2872-65-3 4-methoxyphenyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside 
• 150-76-5 4-methoxy-phenol 
• 144985-19-3 p-methoxyphenyl 3-O-allyl-β-D-galactopyranoside 
• 3150-20-7 4-methoxyphenyl β-D-galactopyranoside 
• 4163-60-4 β-D-galactose peracetate 

Downstream Products

• 1374405-93-2 C₅₄H₆₃NO₁₉ 
• 1237748-32-1 4-methoxyphenyl (2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl)-(1->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 247027-81-2 p-methoxyphenyl 2,4,6-tri-O-benzyl-3-deoxy-3-C-(methylene)-β-D-xylo-hex-3-ulopyranoside 
• 858127-26-1 p-methoxyphenyl 3,4,6-tri-O-benzyl-2-O-methoxycarbonyl-β-D-galactopyranosyl-(1->3)-4,6-O-benzylidene-2-deoxy-2-azido-β-D-galactopyranosyl-(1->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 858127-27-2 2-{7-azido-6-[3,5-bis-benzyloxy-2-benzyloxymethyl-6-(4-methoxy-phenoxy)-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy}-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-3-ol 
• 858127-25-0 (2S,4aR,6S,7R,8R,8aR)-7-Azido-6-[(2R,3S,4S,5R,6S)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-(4-methoxy-phenoxy)-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-ol 
• 858127-24-9 p-methoxyphenyl 3,4,6-tri-O-acetyl-2-deoxy-2-azido-β-D-galactopyranosyl-(1->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 247027-80-1 p-methoxyphenyl 2,4,6-tri-O-benzyl-β-D-xylo-hex-3-ulopyranoside 

Relevant articles and documents

Preparation of acid-resistant heavy fluorous tags for recycling in synthetic systems

Acid-resistant heavy fluorous tags, in which all three fluorous chains are tethered in a symmetric manner by carbon-carbon linkage, were designed and synthesized from ethyl crotonate. They were designed also to possess a reactive OH group at a central position, not only for conjugation with a target molecule but also for tag recycling. The tag with an alkyl spacer equipped the primary OH group had the greatest reactivity in conjugation reactions with target molecules and could be recovered in the highest yields, implying its potential for use in recycling applications.

C-glycoside analogs and methods for their preparation and use

The invention provides versatile sialic acid C-glycoside precursors that are useful for preparing C-glycoside analogs of Gangliosides, peptides, and proteins, as well as synthetic intermediates useful for the preparation of the precursors, and synthetic m