2-Chloro-3-(1,1-difluoroallyl)quinoxaline is a synthetic organic compound characterized by its unique structure, which includes a quinoxaline core, a chlorine substituent, and a difluoroallyl group. The presence of the chlorine atom introduces electrophilic properties, while the difluoroallyl moiety enhances the compound's reactivity and potential for various chemical transformations. This compound may exhibit interesting biological activities due to its structural features, making it a candidate for research in medicinal chemistry. Its fluorinated group can influence lipophilicity and metabolic stability, which are critical factors in drug design. Additionally, the compound's stability, solubility, and reactivity can be affected by the electronic effects of the chlorine and fluorine atoms. As with many quinoxaline derivatives, it may also display potential as a scaffold for developing pharmaceuticals, particularly in the fields of oncology and infectious diseases. However, specific applications and biological activities would require further investigation through experimental studies.

2-chloro-3-(1,1-difluoroallyl)quinoxaline

1294512-27-8: 2-Chloro-3-(1,1-difluoroallyl)quinoxaline is a synthetic organic compound characterized by its unique structure, which includes a quinoxaline core, a chlorine substituent, and a difluoroallyl group. The presence of the chlorine atom introduces electrophilic properties, while the difluoroallyl moiety enhances the compound's reactivity and potential for various chemical transformations. This compound may exhibit interesting biological activities due to its structural features, making it a candidate for research in medicinal chemistry. Its fluorinated group can influence lipophilicity and metabolic stability, which are critical factors in drug design. Additionally, the compound's stability, solubility, and reactivity can be affected by the electronic effects of the chlorine and fluorine atoms. As with many quinoxaline derivatives, it may also display potential as a scaffold for developing pharmaceuticals, particularly in the fields of oncology and infectious diseases. However, specific applications and biological activities would require further investigation through experimental studies.

3-(1,1-difluoroallyl)quinoxalin-2(1H)-one

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CAS 1294512-27-8

2-chloro-3-(1,1-difluoroallyl)quinoxaline

3-(1,1-difluoroallyl)quinoxalin-2(1H)-one

Ref: TR-D473388

3-(1,1-Difluoro-2-propen-1-yl)-2(1H)-quinoxalinone

Ref: 3D-UBC51227