Dimethyl 3,3'-[7,12-bis(1-hydroxyethyl)-3,8,13,17-tetramethylporphyrin-2,18-diyl]dipropanoate is a complex organic compound characterized by its porphyrin structure, which is a cyclic compound composed of four pyrrole subunits interconnected at their α carbon atoms. This specific compound features two propanoate ester groups and hydroxyethyl substituents, contributing to its solubility and reactivity. The presence of multiple methyl groups enhances its hydrophobic character, while the hydroxyl groups provide potential sites for hydrogen bonding and increased polarity. This compound is likely to exhibit interesting photophysical properties, making it relevant in fields such as photodynamic therapy and as a photosensitizer in various chemical reactions. Its intricate structure suggests potential applications in biochemistry and materials science, particularly in the development of sensors or catalysts. As with many porphyrin derivatives, it may also display unique electronic properties, which can be exploited in electronic or optoelectronic devices. Safety and handling precautions should be observed due to its complex nature and potential biological activity.

dimethyl 3,3'-[7,12-bis(1-hydroxyethyl)-3,8,13,17-tetramethylporphyrin-2,18-diyl]dipropanoate

32562-61-1: Dimethyl 3,3'-[7,12-bis(1-hydroxyethyl)-3,8,13,17-tetramethylporphyrin-2,18-diyl]dipropanoate is a complex organic compound characterized by its porphyrin structure, which is a cyclic compound composed of four pyrrole subunits interconnected at their α carbon atoms. This specific compound features two propanoate ester groups and hydroxyethyl substituents, contributing to its solubility and reactivity. The presence of multiple methyl groups enhances its hydrophobic character, while the hydroxyl groups provide potential sites for hydrogen bonding and increased polarity. This compound is likely to exhibit interesting photophysical properties, making it relevant in fields such as photodynamic therapy and as a photosensitizer in various chemical reactions. Its intricate structure suggests potential applications in biochemistry and materials science, particularly in the development of sensors or catalysts. As with many porphyrin derivatives, it may also display unique electronic properties, which can be exploited in electronic or optoelectronic devices. Safety and handling precautions should be observed due to its complex nature and potential biological activity.

CAS 32562-61-1

dimethyl 3,3'-[7,12-bis(1-hydroxyethyl)-3,8,13,17-tetramethylporphyrin-2,18-diyl]dipropanoate

Hematoporphyrin IX dimethyl ester

Ref: FT-H626-9