Boron 4-methyl-3-(2,2,2-trifluoroethoxy)-5H-pyrido[1',2':4,5][1,2,4]thiadiazino[2,3-a]benzimidazol-13-ium fluoride (1:1:4), with CAS number 111712-16-4, is a complex organic compound characterized by its unique structural features, which include a boron atom coordinated to a pyrido-thiadiazino-benzimidazole framework. This compound exhibits properties typical of ionic species, particularly due to the presence of the fluoride ion. The trifluoroethoxy group contributes to its hydrophobic characteristics, potentially influencing its solubility and reactivity in various solvents. The presence of multiple heteroatoms, including nitrogen and sulfur, suggests potential biological activity and reactivity, making it of interest in medicinal chemistry and materials science. Additionally, the compound's unique structure may impart specific electronic properties, which could be exploited in applications such as catalysis or as a ligand in coordination chemistry. Overall, its intricate molecular architecture and functional groups make it a subject of interest for further research in various chemical fields.

boron 4-methyl-3-(2,2,2-trifluoroethoxy)-5H-pyrido[1',2':4,5][1,2,4]thiadiazino[2,3-a]benzimidazol-13-ium fluoride (1:1:4)

111712-16-4: Boron 4-methyl-3-(2,2,2-trifluoroethoxy)-5H-pyrido[1',2':4,5][1,2,4]thiadiazino[2,3-a]benzimidazol-13-ium fluoride (1:1:4), with CAS number 111712-16-4, is a complex organic compound characterized by its unique structural features, which include a boron atom coordinated to a pyrido-thiadiazino-benzimidazole framework. This compound exhibits properties typical of ionic species, particularly due to the presence of the fluoride ion. The trifluoroethoxy group contributes to its hydrophobic characteristics, potentially influencing its solubility and reactivity in various solvents. The presence of multiple heteroatoms, including nitrogen and sulfur, suggests potential biological activity and reactivity, making it of interest in medicinal chemistry and materials science. Additionally, the compound's unique structure may impart specific electronic properties, which could be exploited in applications such as catalysis or as a ligand in coordination chemistry. Overall, its intricate molecular architecture and functional groups make it a subject of interest for further research in various chemical fields.

CAS 111712-16-4

boron 4-methyl-3-(2,2,2-trifluoroethoxy)-5H-pyrido[1',2':4,5][1,2,4]thiadiazino[2,3-a]benzimidazol-13-ium fluoride (1:1:4)

AG 2000

Ref: TM-T29698