The chemical substance known as 2-[3-[1,3-Dihydro-1,3-dimethyl-1-(phenylmethyl)-2H-benz[e]indol-2-ylidene]-1-propen-1-yl]-1,3-dimethyl-1-(phenylmethyl)-1H-benz[e]indolium, with the CAS number 581092-53-7, is a complex organic compound characterized by its intricate structure, which includes multiple aromatic rings and a positively charged indolium moiety. This compound is likely to exhibit properties typical of indole derivatives, such as potential biological activity and photophysical characteristics. The presence of multiple methyl and phenyl groups suggests that it may have enhanced lipophilicity, which could influence its solubility and interaction with biological membranes. Additionally, the compound's structure indicates potential for applications in organic electronics or as a dye, given the conjugated system that may allow for light absorption and emission. Its synthesis and reactivity would be of interest in organic chemistry, particularly in the context of developing new materials or pharmaceuticals. Further studies would be necessary to elucidate its specific properties and potential applications.

2-[3-[1,3-Dihydro-1,3-dimethyl-1-(phenylmethyl)-2H-benz[e]indol-2-ylidene]-1-propen-1-yl]-1,3-dimethyl-1-(phenylmethyl)-1H-benz[e]indolium

581092-53-7: The chemical substance known as 2-[3-[1,3-Dihydro-1,3-dimethyl-1-(phenylmethyl)-2H-benz[e]indol-2-ylidene]-1-propen-1-yl]-1,3-dimethyl-1-(phenylmethyl)-1H-benz[e]indolium, with the CAS number 581092-53-7, is a complex organic compound characterized by its intricate structure, which includes multiple aromatic rings and a positively charged indolium moiety. This compound is likely to exhibit properties typical of indole derivatives, such as potential biological activity and photophysical characteristics. The presence of multiple methyl and phenyl groups suggests that it may have enhanced lipophilicity, which could influence its solubility and interaction with biological membranes. Additionally, the compound's structure indicates potential for applications in organic electronics or as a dye, given the conjugated system that may allow for light absorption and emission. Its synthesis and reactivity would be of interest in organic chemistry, particularly in the context of developing new materials or pharmaceuticals. Further studies would be necessary to elucidate its specific properties and potential applications.

2-[3-[1,3-Dihydro-1,3-dimethyl-1-(phenylmethyl)-2H-benz[e]indol-2-ylidene]-1-propen-1-yl]-1,3-dimethyl-1-(phenylmethyl)-1H-benz[e]indolium hexafluorophosphate(1-) (1

1-Benzyl-2-[3-(1-benzyl-1,3-dimethyl-1H-benzo[e]indol-2(3H)-ylidene)-1-propen-1-yl]-1,3-dimethyl-1H-benzo[e]indol-3-ium Hexafluorophosphate

CAS 581092-53-7

2-[3-[1,3-Dihydro-1,3-dimethyl-1-(phenylmethyl)-2H-benz[e]indol-2-ylidene]-1-propen-1-yl]-1,3-dimethyl-1-(phenylmethyl)-1H-benz[e]indolium

2-[3-[1,3-Dihydro-1,3-dimethyl-1-(phenylmethyl)-2H-benz[e]indol-2-ylidene]-1-propen-1-yl]-1,3-dimethyl-1-(phenylmethyl)-1H-benz[e]indolium hexafluorophosphate(1-) (1

Ref: IN-DA003DZE

1-Benzyl-2-[3-(1-benzyl-1,3-dimethyl-1H-benzo[e]indol-2(3H)-ylidene)-1-propen-1-yl]-1,3-dimethyl-1H-benzo[e]indol-3-ium Hexafluorophosphate

Ref: 54-PC510114