(4aR,7S,8R,8aR)-5-benzyl-2,2-dimethylhexahydro-4H-[1,3]dioxino[5,4-b]pyridine-7,8-diol
95%
Reagent
Code: #57358
CAS Number
114040-86-7
blur_circular Chemical Specifications
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Molecular Information
Weight
293.36 g/mol
Formula
C₁₆H₂₃NO₄
thermostat
Physical Properties
Melting Point
117 °C
Boiling Point
449.9±45.0 °C(Predicted)
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Storage & Handling
Density
1.210±0.06 g/cm3(Predicted)
Storage
room temperature
description Product Description
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of complex bioactive molecules. Its unique structure, featuring a dioxinopyridine core with hydroxyl and benzyl groups, makes it valuable for constructing chiral frameworks in drug development. It is often employed in the preparation of pharmaceuticals targeting neurological disorders, as the scaffold can mimic natural ligands for receptors in the central nervous system. Additionally, its stereochemistry allows for precise control in asymmetric synthesis, enabling the creation of enantiomerically pure compounds. Researchers also explore its potential in developing enzyme inhibitors due to its ability to interact with active sites through hydrogen bonding and hydrophobic interactions. Its applications extend to the design of antiviral and anticancer agents, where its structural complexity contributes to enhanced specificity and efficacy.
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(4aR,7S,8R,8aR)-5-benzyl-2,2-dimethylhexahydro-4H-[1,3]dioxino[5,4-b]pyridine-7,8-diol
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of complex bioactive molecules. Its unique structure, featuring a dioxinopyridine core with hydroxyl and benzyl groups, makes it valuable for constructing chiral frameworks in drug development. It is often employed in the preparation of pharmaceuticals targeting neurological disorders, as the scaffold can mimic natural ligands for receptors in the central nervous system. Additionally, its stereochemistry allows for precise control in asymmetric synthesis, enabling the creation of enantiomerically pure compounds. Researchers also explore its potential in developing enzyme inhibitors due to its ability to interact with active sites through hydrogen bonding and hydrophobic interactions. Its applications extend to the design of antiviral and anticancer agents, where its structural complexity contributes to enhanced specificity and efficacy.
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