129575-89-9

Basic information

• Product Name: 4-METHOXYPHENYL 3,6-DI-O-BENZYL-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE
• Synonyms: 4-Methoxyphenyl 3,6-Di-O-benzyl-2-deoxy-2-phthalimido-β2-((2S,3R,4R,5S,6R)-4-(Benzyloxy)-6-((benzyloxy)methyl)-5-hydroxy-2-(4-methoxyphenoxy)tetrahydro-2H-pyran-3-yl)isoindoline-1,3-dione;4-METHOXYPHENYL 3,6-DI-O-BENZYL-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE;4-Methoxyphenyl 3,6-Di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
• CAS NO: 129575-89-9
• Molecular Formula: C₃₅H₃₃NO₈
• Molecular Weight: 595.64
• Product Categories: Biochemistry;Glucose;Glycosides;N-Substituted Maleimides, Succinimides & Phthalimides;N-Substituted Phthalimides;Sugars
• Mol File: 129575-89-9.mol

Chemical Properties

• Boiling Point: 756.4°C at 760 mmHg
• Flash Point: 411.3°C
• Appearance: /
• Density: 1.35g/cm³
• Vapor Pressure: 4.79E-24mmHg at 25°C
• Refractive Index: 1.66
• Storage Temp.: Freezer
• PKA: 12.82±0.70(Predicted)
• CAS DataBase Reference: 4-METHOXYPHENYL 3,6-DI-O-BENZYL-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHOXYPHENYL 3,6-DI-O-BENZYL-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE(129575-89-9)
• EPA Substance Registry System: 4-METHOXYPHENYL 3,6-DI-O-BENZYL-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE(129575-89-9)

Safety Data

• Hazardous Substances Data: 129575-89-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
4-METHOXYPHENYL 3,6-DI-O-BENZYL-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE is used as a glycoside building block for the synthesis of glycans, which are essential in the development of various pharmaceutical compounds. The compound's unique structure allows for the creation of diverse glycan structures, which can be utilized in the design and synthesis of new drugs targeting specific biological pathways.
Used in Chemical Research:
In the field of chemical research, 4-METHOXYPHENYL 3,6-DI-O-BENZYL-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE serves as an important compound for studying the properties and interactions of glycosides. Its unique structure provides researchers with valuable insights into the behavior of similar compounds and their potential applications in various industries.
Used in Material Science:
4-METHOXYPHENYL 3,6-DI-O-BENZYL-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE can also be utilized in material science for the development of novel materials with specific properties. The compound's unique structure and functional groups can be exploited to create materials with tailored characteristics, such as improved biocompatibility or enhanced mechanical properties.

InChI:InChI=1/C35H33NO8/c1-40-25-16-18-26(19-17-25)43-35-30(36-33(38)27-14-8-9-15-28(27)34(36)39)32(42-21-24-12-6-3-7-13-24)31(37)29(44-35)22-41-20-23-10-4-2-5-11-23/h2-19,29-32,35,37H,20-22H2,1H3/t29-,30-,31-,32-,35-/m1/s1

Upstream product

• 85-44-9 phthalic anhydride 
• 10022-13-6 1,3,4,6-tetra-O-acetyl-2-deoxy-2-phthalimido-D-glucopyranose 
• 100-39-0 benzyl bromide 
• 150-76-5 4-methoxy-phenol 
• 138906-41-9 4-methoxylphenzyl 2-deoxy-2-phthalimido-3,4,6-tri-O-acetyl-β-D-glucopyranoside 
• 138906-43-1 4-methoxyphenyl 4,6-di-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 10022-13-6 1,3,4,6-tetra-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranose 
• 138906-42-0 p-Methoxyphenyl 2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 140615-77-6 4-methoxyphenyl 4-O-acetyl-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 179739-15-2 p-methoxyphenyl 6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 138906-44-2 para-MethoxyPhenyl 3-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 129575-88-8 p-Methoxyphenyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside 

Downstream Products

• 129575-90-2 p-Methoxyphenyl O-(2,4-di-O-acetyl-3,6-di-O-allyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 140615-80-1 p-methoxyphenyl 3,6-di-O-benzyl-4-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 455929-18-7 phenyl 2-O-(2-iodo-1-(p-methoxyphenyl 3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosid-4-O-yl)propyl)-3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside 
• 949000-09-3 C₇₅H₇₅ClN₂O₂₁ 
• 129575-91-3 p-Methoxyphenyl O-(6-O-acetyl-2,4-di-O-benzyl-3-O-levulinoyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 129575-84-4 O-(6-O-Acetyl-2,4-di-O-benzyl-3-O-levulinoyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl trichloroacetimidate 
• 138906-46-4 p-Methoxyphenyl O-(2,4-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 138906-53-3 p-Methoxyphenyl O-(2,4-di-O-benzyl-6-O-pivaloyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 138935-14-5 p-Methoxyphenyl O-(2,4-di-O-benzyl-3-O-levulinoyl-6-O-pivaloyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 134296-64-3 O-(2,4-di-O-Benzyl-3-O-levulinoyl-6-O-pivaloyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl trichloroacetimidate 
• 138935-12-3 p-Methoxyphenyl O-(3,6-di-O-allyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 138906-47-5 p-Methoxyphenyl O-(6-O-acetyl-2,4-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 138906-45-3 p-Methoxyphenyl O-(3,6-di-O-allyl-2,4-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 

Relevant articles and documents

Synthesis of glycosyl acceptors by regioselective benzylations of a 2-deoxy-2-phthalimido-D-glucoside

The direct regioselective benzylation of p-methoxyphenyl 2-deoxy-2-phthalimido-β-D-glucopyranoside (1) with benzyl bromide under basic conditions gives 4,6-di-O-benzyl (2a), 4-O-benzyl (3a) and 6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 4a. When

Ionic-liquid supported rapid synthesis of an: N -glycan core pentasaccharide on a 10 g scale

A new and efficient Ionic Liquid-Supported Oligosaccharide Synthesis (ILSOS) strategy for an N-linked core pentasaccharide on a 10 g scale is reported. This new ILSOS includes a new spacer for an IL support, a new tagging strategy, and fast, efficient and orthogonal removal of the ionic-liquid support, producing the N-linked core pentasaccharide with direct applicability potential in a short time, with high yield and on a large gram scale.

Chemoenzymatic approach for the preparation of asymmetric bi-, tri-, and tetra-antennary N-glycans from a common precursor

Progress in glycoscience is hampered by a lack of well-defined complex oligosaccharide standards that are needed to fabricate the next generation of microarrays, to develop analytical protocols to determine exact structures of isolated glycans, and to elu

Preparation of Thiosugars and Their Use

A process for the preparation of a thiosaccharide represented by Saccharide-S-H wherein Saccharide comprises at least 4 sugar units, comprises subjecting a corresponding compound of the formula (P)Saccharide-S-(P) wherein (P) represents an O- or S-protecting group(s), to Birch reduction.

Use of methanesulfonic acid in the reductive ring-opening of O-benzylidene acetals

Methanesulfonic acid was shown to be an efficient and convenient substitute for ethereal HCl in reductive 4,6-O-benzylidene acetal ring-opening reaction with sodium cyanoborohydride in THF. Normal regioselectivity was observed, the 6-O-benzyl ethers with

Synthesis of sulfated glucuronyl glycosphingolipids; carbohydrate epitopes of neural cell-adhesion molecules

The sulfated glucuronyl glycosphingolipids isolated from the human peripheral nervous system, HO3S-3-β-GlcpA-(1 → 3)-{β-D-Galp-(1 → 4)-β-D-GlcpNAc-(1 → 3)}(n)-β-D-Galp-(1 → 4)-β-D-Glcp-(1 → 1)-Cer (n = 1, 2) (1 and 2) were synthesized. The glyc

Total synthesis of a sulfated glucuronyl glycosphingolipid, IV3GlcA(3-SO3)nLcOse4Cer, a carbohydrate epitope of neural cell adhesion molecules

A total synthesis of a sulfated glucuronyl glycosphingolipid isolated from human peripheral nervous system was achieved for the first time.