905588-87-6

Basic information

• Product Name: 2,6-bis{2-[(tert-butyldiphenylsilyl)oxy]ethoxy}-9-[4,5-bis(5-chloropentylsulfanyl)-1,3-dithiol-2-ylidene]-10-[4,5-bis(2-cyanoethylsulfanyl)-1,3-dithiol-2-ylidene]-9,10-dihydroanthracene
• Synonyms: 2,6-bis{2-[(tert-butyldiphenylsilyl)oxy]ethoxy}-9-[4,5-bis(5-chloropentylsulfanyl)-1,3-dithiol-2-ylidene]-10-[4,5-bis(2-cyanoethylsulfanyl)-1,3-dithiol-2-ylidene]-9,10-dihydroanthracene
• CAS NO: 905588-87-6
• Molecular Weight: 1421.04
• Mol File: 905588-87-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,6-bis{2-[(tert-butyldiphenylsilyl)oxy]ethoxy}-9-[4,5-bis(5-chloropentylsulfanyl)-1,3-dithiol-2-ylidene]-10-[4,5-bis(2-cyanoethylsulfanyl)-1,3-dithiol-2-ylidene]-9,10-dihydroanthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-bis{2-[(tert-butyldiphenylsilyl)oxy]ethoxy}-9-[4,5-bis(5-chloropentylsulfanyl)-1,3-dithiol-2-ylidene]-10-[4,5-bis(2-cyanoethylsulfanyl)-1,3-dithiol-2-ylidene]-9,10-dihydroanthracene(905588-87-6)
• EPA Substance Registry System: 2,6-bis{2-[(tert-butyldiphenylsilyl)oxy]ethoxy}-9-[4,5-bis(5-chloropentylsulfanyl)-1,3-dithiol-2-ylidene]-10-[4,5-bis(2-cyanoethylsulfanyl)-1,3-dithiol-2-ylidene]-9,10-dihydroanthracene(905588-87-6)

Safety Data

• Hazardous Substances Data: 905588-87-6(Hazardous Substances Data)

Upstream product

• 345915-46-0 2,6-bis(2-tercbutyldiphenylsilyloxyethyloxy)-9,10-anthraquinone 
• 193148-62-8 4,5-bis(5-chloropentylsulfanyl)-1,3-dithiole-2-thione 
• 132765-35-6 4,5-bis((2-cyanoethyl)thio)-1,3-dithiole-2-thione 

Downstream Products

• 905588-88-7 2,6-bis{2-[(tert-butyldiphenylsilyl)oxy]ethoxy}-9-[4,5-bis(2-cyanoethylsulfanyl)-1,3-dithiol-2-ylidene]-10-[4,5-bis(5-iodopentylsulfanyl)-1,3-dithiol-2-ylidene]-9,10-dihydroanthracene 

Relevant articles and documents

Extreme conformational constraints in π-extended tetrathiafulvalenes: Unusual topologies and redox behavior of doubly and triply bridged cyclophanes

Doubly and triply bridged 9,10-bis(1,3-dithiol-2-ylidene)-9,10- dihydroanthracene (ex-TTF) derivatives have been synthesized. Key steps are the generation and macrocyclization reactions of ex-TTF-dithiolate reagents. The X-ray crystal structures of the do