1440762-38-8

Basic information

• Product Name: N,N’-bis(1-ethylpropyl)-2-(4-tert-butylacetanilide-2-yl)perylene-3,4:9,10-tetracarboxylic acid bisimide
• Synonyms: N,N’-bis(1-ethylpropyl)-2-(4-tert-butylacetanilide-2-yl)perylene-3,4:9,10-tetracarboxylic acid bisimide
• CAS NO: 1440762-38-8
• Molecular Weight: 719.88
• Mol File: 1440762-38-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N,N’-bis(1-ethylpropyl)-2-(4-tert-butylacetanilide-2-yl)perylene-3,4:9,10-tetracarboxylic acid bisimide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N’-bis(1-ethylpropyl)-2-(4-tert-butylacetanilide-2-yl)perylene-3,4:9,10-tetracarboxylic acid bisimide(1440762-38-8)
• EPA Substance Registry System: N,N’-bis(1-ethylpropyl)-2-(4-tert-butylacetanilide-2-yl)perylene-3,4:9,10-tetracarboxylic acid bisimide(1440762-38-8)

Safety Data

• Hazardous Substances Data: 1440762-38-8(Hazardous Substances Data)

Upstream product

• 110590-81-3 N,N'-bis(1-ethylpropyl)-3,4:9,10-perylenebis(dicarboximide) 
• 1294450-29-5 N,N’-bis(1-ethylpropyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)perylene-3,4:9,10-tetracarboxylic acid bisimide 
• 91801-97-7 N-(2-bromo-4-tert-butylphenyl)acetamide 

Relevant articles and documents

Synthesis of pyridine-fused perylene imides with an amidine moiety for hydrogen bonding

Pyridine-fused perylene tetracarboxylic acid bisimides (PBIs) were synthesized via Suzuki-Miyaura coupling and acid condensation. The fused PBIs with electron-donating substituents exhibited an intramolecular charge transfer interaction. One of the N-alkyl substituents was selectively removed with BBr3 to create an amidine guest binding site. A hydrogen bonding interaction with pentafluorobenzoic acid changed the absorption spectra and enhanced fluorescence.