2646-97-1

Usage

Uses

Used in Pharmaceutical Industry:
NSC221148 is used as a chemical precursor for the synthesis of various biologically active compounds, contributing to the development of new drugs and therapies.
Used in Cancer Treatment:
NSC221148 is used as a potential therapeutic agent for the treatment of various types of cancer, including its application in photodynamic therapy.
Used in Neurological Disorders:
NSC221148 is used in research for its potential role in the treatment of neurological disorders, offering a new avenue for therapeutic intervention.
Used in Antimicrobial Applications:
NSC221148 is used in the development of antimicrobial agents, providing an alternative solution to combat resistant bacteria.
Used in Antiviral Applications:
NSC221148 is used in the research and development of antiviral agents, offering potential treatments for viral infections.
Used in Scientific Research:
NSC221148 is used as a versatile compound in various scientific research endeavors, aiding in the discovery and understanding of new biological processes and mechanisms.

InChI:InChI=1/C7H6F3N.ClH/c8-7(9,10)5-2-1-3-6(11)4-5;/h1-4H,11H2;1H

Upstream product

• 98-08-8 α,α,α-trifluorotoluene 

Downstream Products

• 129158-00-5 6-Benzyl-2,5-dimethyl-3-(3-trifluoromethyl-phenyl)-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one 
• 351-36-0 N-acetyl-3-trifluoromethylbenzenamine 
• 368-78-5 3-(trifluoromethyl)phenylhydrazine 
• 34648-94-7 m-trifluoromethyldiazonium chloride 
• 1245643-77-9 ethyl 1-(3-(trifluoromethyl)phenyl)-1H-1,2,4-triazole-3-carboxylate 
• 34556-78-0 3-(trifluoromethyl)-N-[3-(trifluoromethyl)phenyl]benzamide 
• 1403665-00-8 6-benzyl-10-trifluoromethylquino[3,2-b]benzothiazine 
• 146898-62-6 3,5-bis(4-fluorophenyl)-4-(3-(trifluoromethyl)phenyl)-1,2,4-triazole 
• 100633-91-8 4-(N-(3-trifluoromethylphenyl)amino)-5,6 dimethyl-7H-pyrrolo[2.3-d]pyrimidine 

Relevant academic research and scientific papers

Pyridyl Radical Cation for C?H Amination of Arenes

Electron-transfer photocatalysis provides access to the elusive and unprecedented N-pyridyl radical cation from selected N-substituted pyridinium reagents. The resulting C(sp2)?H functionalization of (hetero)arenes furnishes versatile intermediates for the development of valuable aminated aryl scaffolds. Mechanistic studies that include the first spectroscopic evidence of a spin-trapped N-pyridyl radical adduct implicate SET-triggered, pseudo-mesolytic cleavage of the N?X pyridinium reagents mediated by visible light.