116308-18-0

Usage

Uses

Used in Organic Synthesis:
(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 used as a key intermediate in organic synthesis for the development of new compounds with specific properties. Its unique structure allows for various chemical reactions, making it a valuable building block in the creation of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (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 utilized as a precursor for the synthesis of pharmaceutically active compounds. Its multi-functionalized nature enables the design and synthesis of novel drug candidates with potential therapeutic applications.
Used in Research and Development:
(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 serves as a valuable compound in research and development settings. Its synthesis and characterization provide insights into the properties and potential uses of complex organic molecules, contributing to the advancement of scientific knowledge in chemistry and related fields.

Upstream product

• 116308-14-6 2,3,4,6-Tetra-O-benzyl-1-C-(dichloromethyl)-D-glucitol 
• 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 

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 academic research and scientific papers

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.