Ethyl 4-[4-(difluoromethoxy)phenyl]-2-methyl-5-oxo-1,4,5,7-tetrahydrofuro[3,4-b]pyridine-3-carboxylate, with the CAS number 92638-14-7, is a synthetic organic compound characterized by its complex molecular structure, which includes a pyridine ring fused with a furo[3,4-b] moiety. This compound features a carboxylate ester functional group, contributing to its potential reactivity and solubility properties. The presence of a difluoromethoxy group enhances its lipophilicity and may influence its biological activity. Typically, compounds of this nature are investigated for their pharmacological properties, including potential applications in medicinal chemistry. The structural intricacies suggest that it may exhibit specific interactions with biological targets, making it a candidate for further research in drug development. Additionally, the compound's stability, solubility, and reactivity can be influenced by the substituents on the aromatic rings and the overall molecular conformation. As with many synthetic compounds, safety and handling precautions are essential when working with this substance in a laboratory setting.

ethyl 4-[4-(difluoromethoxy)phenyl]-2-methyl-5-oxo-1,4,5,7-tetrahydrofuro[3,4-b]pyridine-3-carboxylate

92638-14-7: Ethyl 4-[4-(difluoromethoxy)phenyl]-2-methyl-5-oxo-1,4,5,7-tetrahydrofuro[3,4-b]pyridine-3-carboxylate, with the CAS number 92638-14-7, is a synthetic organic compound characterized by its complex molecular structure, which includes a pyridine ring fused with a furo[3,4-b] moiety. This compound features a carboxylate ester functional group, contributing to its potential reactivity and solubility properties. The presence of a difluoromethoxy group enhances its lipophilicity and may influence its biological activity. Typically, compounds of this nature are investigated for their pharmacological properties, including potential applications in medicinal chemistry. The structural intricacies suggest that it may exhibit specific interactions with biological targets, making it a candidate for further research in drug development. Additionally, the compound's stability, solubility, and reactivity can be influenced by the substituents on the aromatic rings and the overall molecular conformation. As with many synthetic compounds, safety and handling precautions are essential when working with this substance in a laboratory setting.

<p>Cgp 28861 reverses the effects of calcium channel blockaders in the frog heart.</p>

CAS 92638-14-7

ethyl 4-[4-(difluoromethoxy)phenyl]-2-methyl-5-oxo-1,4,5,7-tetrahydrofuro[3,4-b]pyridine-3-carboxylate

Cgp 28861

Ref: TM-T30823