CAS 681482-81-5
:Phenol, 4-[4-[4-(trifluoromethoxy)phenoxy]-1-piperidinyl]-
Description:
The chemical substance known as "Phenol, 4-[4-[4-(trifluoromethoxy)phenoxy]-1-piperidinyl]-" with CAS number 681482-81-5 is a complex organic compound characterized by its phenolic structure and the presence of a piperidine ring. This compound features a trifluoromethoxy group, which contributes to its unique chemical properties, including increased lipophilicity and potential biological activity. The presence of multiple aromatic rings enhances its stability and may influence its interactions with biological targets. Typically, such compounds are investigated for their potential applications in pharmaceuticals, particularly in the development of therapeutic agents. The trifluoromethoxy group can also enhance the compound's metabolic stability and bioavailability. Additionally, the compound may exhibit specific solubility characteristics, making it suitable for various formulations. Overall, this substance represents a class of compounds that are of interest in medicinal chemistry due to their potential efficacy and specificity in biological systems.
Formula:C18H18F3NO3
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Found 6 products.
4-(4-[4-(Trifluoromethoxy)phenoxy]piperidino)benzenol
CAS:Formula:C18H18F3NO3Purity:98%Color and Shape:SolidMolecular weight:353.33564-(4-(4-(Trifluoromethoxy)phenoxy)piperidin-1-yl)phenol
CAS:4-(4-(4-(Trifluoromethoxy)phenoxy)piperidin-1-yl)phenolPurity:98%Molecular weight:353.34g/mol4-[4-(4-Trifluoromethoxyphenoxy)piperidin-1-yl]phenol
CAS:Controlled Product<p>Applications 4-[4-(4-Trifluoromethoxyphenoxy)piperidin-1-yl]phenol is an intermediate in the synthesis of Delamanid (D230660), a novel anti-tuberculosis medication that inhibits mycolic acid synthesis and shows potent in-vitro and in-vivo activity against drug-resistant strains of Mycobacterium tuberculosis.<br>References Sasaki, H., et al.: J. Med. Chem., 49, 7854 (2006);<br></p>Formula:C18H18F3NO3Color and Shape:NeatMolecular weight:353.34





