1286685-59-3

Basic information

• Product Name: [4-(2-{4-[7-(5,5-dimethyl[1,3]dioxin-2-yl)-2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl]phenyl}-vinyl)-phenyl]-diphenyl-amine
• Synonyms: [4-(2-{4-[7-(5,5-dimethyl[1,3]dioxin-2-yl)-2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl]phenyl}-vinyl)-phenyl]-diphenyl-amine
• CAS NO: 1286685-59-3
• Molecular Weight: 601.766
• Mol File: 1286685-59-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [4-(2-{4-[7-(5,5-dimethyl[1,3]dioxin-2-yl)-2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl]phenyl}-vinyl)-phenyl]-diphenyl-amine(CAS DataBase Reference)
• NIST Chemistry Reference: [4-(2-{4-[7-(5,5-dimethyl[1,3]dioxin-2-yl)-2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl]phenyl}-vinyl)-phenyl]-diphenyl-amine(1286685-59-3)
• EPA Substance Registry System: [4-(2-{4-[7-(5,5-dimethyl[1,3]dioxin-2-yl)-2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl]phenyl}-vinyl)-phenyl]-diphenyl-amine(1286685-59-3)

Safety Data

• Hazardous Substances Data: 1286685-59-3(Hazardous Substances Data)

Upstream product

• 204905-77-1 3,4-ethylenedioxythiophene-2-carboxaldehyde 
• 126213-50-1 3,4-(ethylenedioxy)thiophene 
• 1286685-28-6 {4-[7-(5,5-dimethyl[1,3]dioxan-2-yl)2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl]-benzyl}phosphonic acid diethyl ester 
• 4181-05-9 4-(diphenylamino)benzaldehyde 
• 1286685-27-5 5-bromo-7-(5,5-dimethyl[1,3]dioxin-2-yl)-2,3-dihydrothieno[3,4-b][1,4]dioxine 
• 1286685-26-4 5-(5,5-dimethyl-[1,3]dioxin-2-yl)-2,3-dihydro-thieno[3,4-b][1,4]dioxine 

Downstream Products

• 1286685-65-1 7-{4-[2-(4-diphenylamino-phenyl)-vinyl]phenyl}-2,3-dihydrothieno[3,4-b][1,4]dioxin-5-carbaldehyde 
• 1286685-67-3 [4-(2-{4-[7-(2-{4-[7-(5,5-dimethyl-[1,3]dioxan-2-yl)-9,9-dioctyl-9H-fluorene-2-yl]-phenyl}-vinyl)-2,3-dihydro-thieno[3,4-b][1,4]dioxin-5-yl]-phenyl}-vinyl)-phenyl]-diphenylamine 

Relevant articles and documents

Harnessing "click"-type chemistry for the preparation of novel electronic materials

Sequence-independent or "click"-type chemistry is applied for the preparation of novel π-conjugated oligomers. A variety of bi-functional monomers for Wittig-Horner olefination are developed and applied in a sequential protection-deprotection process for the preparation of structurally similar π-conjugated oligomers. Selected oligomers are incorporated as the organic semiconductors in light-emitting diodes and a field-effect transistor, demonstrating the potential of the approach. Sequence-independent or "click"-type chemistry is applied for the preparation of novel π-conjugated oligomers. A variety of bi-functional monomers for Wittig-Horner olefination are developed and applied in a sequential protection-deprotection process for the preparation of structurally similar π-conjugated oligomers. Selected oligomers are incorporated as the organic semiconductors in light-emitting diodes and a field-effect transistor, demonstrating the potential of the approach.