313652-89-0

Basic information

• Product Name: meso-(4-dodecyloxytphen-1-yl)-2,2’-dipyrromethane
• Synonyms: meso-(4-dodecyloxytphen-1-yl)-2,2’-dipyrromethane
• CAS NO: 313652-89-0
• Molecular Weight: 406.612
• Mol File: 313652-89-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: meso-(4-dodecyloxytphen-1-yl)-2,2’-dipyrromethane(CAS DataBase Reference)
• NIST Chemistry Reference: meso-(4-dodecyloxytphen-1-yl)-2,2’-dipyrromethane(313652-89-0)
• EPA Substance Registry System: meso-(4-dodecyloxytphen-1-yl)-2,2’-dipyrromethane(313652-89-0)

Safety Data

• Hazardous Substances Data: 313652-89-0(Hazardous Substances Data)

Upstream product

• 109-97-7 pyrrole 
• 24083-19-0 4-n-dodecyloxybenzaldehyde 
• 143-15-7 1-dodecylbromide 
• 414866-50-5 meso-(4-hydroxyphenyl)dipyrromethane 

Relevant articles and documents

Hexameric and pentameric slipped-cofacial dimers: Toward an artificial light-harvesting complex

(Chemical Equation Presented) We prepared a zinc complex of bis(1-methylimidazolyl)-m-gable porphyrin. The automatically assembled coordinate species showed a complex mixture of wide molecular weight distributions accompanied with assemblies of specific a

Trans-A2B2 porphyrin derivative, and preparation method and application thereof

The invention discloses a trans-A2B2 porphyrin derivative, and a preparation method and an application thereof. The preparation method comprises the following steps: carrying out a reaction on 4-alkoxybenzaldehyde and pyrrole under the catalysis of trifluoroacetic acid to synthesize 5-substituted dipyrrylmethane; carrying out a cyclization reaction on the obtained 5-substituted dipyrrylmethane and 5-bromo-2-thiophenecarboxaldehyde under the action of trifluoroacetic acid and dichlorodicyan benzoquinone to form a porphyrin ring main body; connecting the thiophene alpha position of the porphyrin ring with a boronic acid pinacol ester group through using a Suzuki coupling reaction to modify the porphyrin ring; and carrying out the Suzuki coupling reaction on bromodicyanovinyl oligothiophene prepared in the early stage and the modified porphyrin ring under the catalysis action of palladium to obtain the final product. The trans-A2B2 porphyrin derivative is hopeful to become a high-efficiency organic photovoltaic battery donor material due to the unique molecular structure and large conjugated system.