152169-45-4

Usage

Molecular structure

A phenolic compound with two fluorine atoms (F) and a pivaloylamino group (C(CH3)3) attached to the phenol ring, and a tetrahydropyranyl group (C5H8O) linked to the O atom of the phenol.

Potential applications

The compound may have antifungal or antibacterial properties, and its structure suggests potential bioactivity for use as a therapeutic agent in the pharmaceutical industry.

Need for further research

More research is needed to fully understand the compound's potential applications and mechanisms of action.

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 152169-44-3 2,4-difluoro-5-pivaloylaminophenol 
• 367-27-1 2,4-difluorophenol 
• 152169-43-2 2,4-difluorophenyl ethyl carbonate 
• 113512-57-5 2,4-difluoro-5-nitrophenol 
• 113512-71-3 2,4-difluoro-5-hydroxyaniline 

Downstream Products

• 152835-78-4 ethyl 3,5-difluoro-6-(N-pivaloylamino)-2-(2-tetrahydropyranyloxy)benzoate 
• 152169-56-7 5-amino-2-(4-amino-3-fluorophenyl)-6,8-difluoro-4H-1-benzopyran-4-one 
• 152835-71-7 6,8-Difluoro-2-(3-fluoro-4-pivaloylaminophenyl)-5-pivaloylamino-4H-1-benzopyran-4-one 
• 152835-84-2 ethyl 3,5-difluoro-6-pivaloylamino-2-(2-tetrahydropyranyloxy)-4-trimethylsilylbenzoate 
• 152169-46-5 2,4-difluoro-5-pivaloylamino-3-trimethylsilyl-O-(2-tetrahydropyranyl)phenol 

Relevant academic research and scientific papers

Synthesis of an ethyl 6-amino-3,5-difluorosalicylate derivative by sequential regioselective directed ortho- metalation; a practical synthesis of 4',5-Diamino-3',6,8-trifluoroflavone, a potent antitumor agent

The multigram scale synthesis of 4',5-diamino-3'6,8-trifluoroflavone, a potent antitumor agent, is described in which regioselective introduction of a carbonyl group into the ortho-position to the amide group of 2-[2,4-difluoro-5-(pivaloylamino)phenyoxy]tetrahydropyran is achieved by using sequential direct ortho-metalations as the key step.

5-aminoflavone derivatives

5-Aminoflavone derivatives represented by the formula (I): STR1 wherein R1, R2, R3 and R4 are the same or different and represent hydrogen, substituted or unsubstituted lower alkyl, lower alkenyl, halogen-substi

5-Aminoflavone derivatives, their preparation and their use as antibacterial, anti-estrogenic and/or antitumor agent

5-Aminoflavone derivatives represented by the formula (I): wherein R1 and R2 are the same or different and represent hydrogen or substituted or unsubstituted lower alkyl, X represents substituted or unsubstituted lower alkyl, lower alkenyl, lower alkynyl,