116308-18-0

Basic information

• Product Name: (1S)-(1(OH),2,4/1,3)-2,3,4-Tri-O-benzyl-1-C-<(benzyloxy)methyl>-6,6-dichloro-5-oxo-1,2,3,4-cyclohexanetetrol
• Synonyms: (1S)-(1(OH),2,4/1,3)-2,3,4-Tri-O-benzyl-1-C-<(benzyloxy)methyl>-6,6-dichloro-5-oxo-1,2,3,4-cyclohexanetetrol
• CAS NO: 116308-18-0
• Molecular Weight: 621.557
• Mol File: 116308-18-0.mol
• Article Data: 2

Chemical Properties

• Melting Point: 139-142 °C
• Boiling Point: 723.4±60.0 °C(Predicted)
• Density: 1.31±0.1 g/cm3(Predicted)
• CAS DataBase Reference: (1S)-(1(OH),2,4/1,3)-2,3,4-Tri-O-benzyl-1-C-<(benzyloxy)methyl>-6,6-dichloro-5-oxo-1,2,3,4-cyclohexanetetrol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S)-(1(OH),2,4/1,3)-2,3,4-Tri-O-benzyl-1-C-<(benzyloxy)methyl>-6,6-dichloro-5-oxo-1,2,3,4-cyclohexanetetrol(116308-18-0)
• EPA Substance Registry System: (1S)-(1(OH),2,4/1,3)-2,3,4-Tri-O-benzyl-1-C-<(benzyloxy)methyl>-6,6-dichloro-5-oxo-1,2,3,4-cyclohexanetetrol(116308-18-0)

Safety Data

• Hazardous Substances Data: 116308-18-0(Hazardous Substances Data)

Usage

General Description

(1S)-(1(OH),2,4/1,3)-2,3,4-Tri-O-benzyl-1-C-<(benzyloxy)methyl>-6,6-dichloro-5-oxo-1,2,3,4-cyclohexanetetrol is a complex chemical compound with a cyclohexane backbone and multiple benzyl and chloro substituents. The compound also contains a benzyloxy-methyl group attached to the carbon at position 1. It is a multi-functionalized molecule with potential applications in organic synthesis and medicinal chemistry due to its unique structure and reactivity. (1S)-(1(OH),2,4/1,3)-2,3,4-Tri-O-benzyl-1-C-<(benzyloxy)methyl>-6,6-dichloro-5-oxo-1,2,3,4-cyclohexanetetrol's precise synthesis and characterization are essential for understanding its properties and potential uses in various fields.

Upstream product

• 140658-50-0 (2R,3R,4S,5R,6R)-3,4,5-tris-benzyl-6-benzyloxymethyl-2-dichloromethyltetrahydro-2H-pyran-2-ol 
• 13096-62-3 (3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-one 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 131531-76-5 p-methylphenyl 2,3,4,6-tetra-O-benzyl-thio-β-D-glucopyranoside 
• 28244-94-2 p-tolyl-2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside 
• 116308-14-6 2,3,4,6-Tetra-O-benzyl-1-C-(dichloromethyl)-D-glucitol 

Downstream Products

• 115250-39-0 (1S)-(1(OH),2,4,5/1,3)-2,3,4-tri-O-benzyl-5-<<2-hydroxy-1-(hydroxymethyl)ethyl>amino>-1-C-<(benzyloxy)methyl>-1,2,3,4-cyclohexanetetrol 
• 83480-29-9 voglibose 
• 140676-23-9 (1S)-(1(OH),2,4,5/1,3)-2,3,4-Tri-O-benzyl-1-C-<(benzyloxy)methyl>-1,2,3,4,5-cyclohexanepentol 
• 115250-26-5 (1S)-(1(OH),2,4,5/1,3)-1-C-(Hydroxymethyl)-1,2,3,4,5-cyclohexanepentol 
• 116308-02-2 (1S)-(1(OH),2,4,6/1,3)-2,3,4-Tri-O-benzyl-1-C-<(benzyloxy)methyl>-6-chloro-5-oxo-1,2,3,4-cyclohexanetetrol 
• 115250-38-9 (1S)-(1(OH),2,4/1,3)-2,3,4-Tri-O-benzyl-1-C-<(benzyloxy)methyl>-5-oxo-1,2,3,4-cyclohexanetetrol 

Relevant articles and documents

Synthesis method of voglibose

The invention provides a synthesis method of voglibose, and solves the technical problems that in an existing synthesis method of voglibose, raw materials are difficult to obtain, high in price, large in investment, low in yield and not suitable for industrial production. The synthesis method comprises the steps: synthesizing a compound V by taking glucose monohydrate and sodium acetate as raw materials through eleven reaction steps; and preparing a compound VIII from the compound V through an addition reaction, a ring-opening reaction and an aldol condensation reaction, and thus obtaining voglibose through amination reduction of the compound VIII. The synthesis method of voglibose can be widely applied to the technical field of voglibose synthesis methods.