126473-59-4

Basic information

• Product Name: 1-Ethyl-2-{(1E,3E,5E)-7-[1-ethyl-3,3-dimethyl-1,3-dihydro-indol-(2Z)-ylidene]-hepta-1,3,5-trienyl}-3,3-dimethyl-5-[4-((1Z,4Z,9Z,15Z)-10,15,20-triphenyl-porphyrin-5-yl)-phenylcarbamoyl]-3H-indolium; iodide
• Synonyms: 1-Ethyl-2-{(1E,3E,5E)-7-[1-ethyl-3,3-dimethyl-1,3-dihydro-indol-(2Z)-ylidene]-hepta-1,3,5-trienyl}-3,3-dimethyl-5-[4-((1Z,4Z,9Z,15Z)-10,15,20-triphenyl-porphyrin-5-yl)-phenylcarbamoyl]-3H-indolium; iodide
• CAS NO: 126473-59-4
• Molecular Weight: 1220.31
• Mol File: 126473-59-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-Ethyl-2-{(1E,3E,5E)-7-[1-ethyl-3,3-dimethyl-1,3-dihydro-indol-(2Z)-ylidene]-hepta-1,3,5-trienyl}-3,3-dimethyl-5-[4-((1Z,4Z,9Z,15Z)-10,15,20-triphenyl-porphyrin-5-yl)-phenylcarbamoyl]-3H-indolium; iodide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Ethyl-2-{(1E,3E,5E)-7-[1-ethyl-3,3-dimethyl-1,3-dihydro-indol-(2Z)-ylidene]-hepta-1,3,5-trienyl}-3,3-dimethyl-5-[4-((1Z,4Z,9Z,15Z)-10,15,20-triphenyl-porphyrin-5-yl)-phenylcarbamoyl]-3H-indolium; iodide(126473-59-4)
• EPA Substance Registry System: 1-Ethyl-2-{(1E,3E,5E)-7-[1-ethyl-3,3-dimethyl-1,3-dihydro-indol-(2Z)-ylidene]-hepta-1,3,5-trienyl}-3,3-dimethyl-5-[4-((1Z,4Z,9Z,15Z)-10,15,20-triphenyl-porphyrin-5-yl)-phenylcarbamoyl]-3H-indolium; iodide(126473-59-4)

Safety Data

• Hazardous Substances Data: 126473-59-4(Hazardous Substances Data)

Upstream product

• 126442-89-5 5-(4-acetamidophenyl)-10,15,20-tris(phenyl)porphyrin 
• 126442-88-4 1,1'-diethyl-3,3,3',3'-tetramethyl-5-carboxyindotricarbocyanine iodide 
• 67605-64-5 5-(p-aminophenyl)-10,15,20-triphenylporphine 
• 109-97-7 pyrrole 
• 100-52-7 benzaldehyde 
• 126442-94-2 1-Ethyl-2-{(1E,3E,5E)-7-[1-ethyl-3,3-dimethyl-1,3-dihydro-indol-(2Z)-ylidene]-hepta-1,3,5-trienyl}-5-(4-formyl-phenylcarbamoyl)-3,3-dimethyl-3H-indolium; iodide 

Relevant articles and documents

VISIBLE LIGTH-HARVESTING IN COVALENTLY-LINKED PORPHYRIN-CYANINE DYES

We report the synthesis and properties if three members of a new class of photochemical model compounds containing a covalently-linked porphyrin and a cyanide dye.In compounds 1 and 2 the dye absorbs in the 450-570 nm region and energy transfer occurs with 80percent efficiency from the dye to the free base porphyrin.In compound 3 the dye absorbs in the 650-780 nm region and energy transfer occurs with 80percent efficiency from the free base porphyrin to the dye.The zinc-porphyrin-dyes exhibit both donor and acceptor quenching with only moderate yields of energy transfer.This work is a first step toward the development of an artificial phycobilisome.