600717-91-7

Basic information

• Product Name: 1,3-Dithiole, 2-[4-[[[4-(bromomethyl)cyclohexyl]methyl]thio]-1,3-dithiol-2-ylidene]-4,5- bis[(2-ethylbutyl)thio]-
• CAS NO: 600717-91-7
• Molecular Formula: C26H41BrS7
• Molecular Weight: 657.978
• Mol File: 600717-91-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,3-Dithiole, 2-[4-[[[4-(bromomethyl)cyclohexyl]methyl]thio]-1,3-dithiol-2-ylidene]-4,5- bis[(2-ethylbutyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dithiole, 2-[4-[[[4-(bromomethyl)cyclohexyl]methyl]thio]-1,3-dithiol-2-ylidene]-4,5- bis[(2-ethylbutyl)thio]-(600717-91-7)
• EPA Substance Registry System: 1,3-Dithiole, 2-[4-[[[4-(bromomethyl)cyclohexyl]methyl]thio]-1,3-dithiol-2-ylidene]-4,5- bis[(2-ethylbutyl)thio]-(600717-91-7)

Safety Data

• Hazardous Substances Data: 600717-91-7(Hazardous Substances Data)

Upstream product

• 600717-86-0 3-[4',5'-bis-(2-ethyl-butylsulfanyl)-[2,2']bi[[1,3]dithiolylidene]-4-ylsulfanyl]-propionitrile 
• 35541-75-4 1,4-bis-(bromomethyl)cyclohexane 

Downstream Products

• 600717-95-1 C-{4-[4',5'-bis-(2-ethyl-butylsulfanyl)-[2,2']bi[[1,3]dithiolylidene]-4-ylsulfanylmethyl]-cyclohexyl}-methylamine 
• 600717-93-9 4'-(4-azidomethyl-cyclohexylmethylsulfanyl)-4,5-bis-(2-ethyl-butylsulfanyl)-[2,2']bi[[1,3]dithiolylidene] 

Relevant articles and documents

Donor-acceptor-donor triads incorporating tetrathiafulvalene and perylene diimide units: Synthesis, electrochemical and spectroscopic studies

Three donor-acceptor-donor triads 1-3 consisting of tetrathiafulvalene units attached to perylene diimides by flexible and rigid spacers were synthesized and characterized. UV/vis spectroscopic and cyclic voltammetric results indicate that they all show negligible intramolecular charge transfer interaction in their ground states. As compared to the reference compound 21, triads 1-3 display reduced fluorescence and their fluorescence lifetimes are shortened, which is probably owing to the photoinduced electron transfer interactions between the PI units and TTF units. The different photophysical behaviors between 1 and 2 (and 3) might be due to their difference in the spatial separation of TTF and PI units. It is preliminarily found that the steric hindrance of the groups attached to TTF units can affect their photostability.