33955-42-9

Usage

Ketone groups

The chemical contains four ketone groups at positions 1, 3, 8, and 10, which contribute to its unique chemical properties.

Fused rings

The compound has a benzopyran ring system fused to an anthraquinone and an isoquinoline ring, which gives it a complex and structurally interesting nature.

Interest to synthetic chemists

The complex structure of 1H-2-Benzopyrano(6,5,4:10,5,6)anthra(2,1,9-def)isoquinoline-1,3,8,10(9H)-tetrone may make it of interest to synthetic chemists for studying complex organic transformations and reactions, potentially leading to advancements in organic chemistry.

Upstream product

• 128-69-8 perylene-3,4,9,10-tetracarboxylic acid 3,4:9,10-dianhydride 

Downstream Products

• 130296-50-3 N²-(2,5-Di-tert-butylphenyl)-3,4:9,10-perylentetracarboxdiimid 
• 33955-44-1 perylene-3,4-dicarboximide 
• 1438842-16-0 N-3,4,5-tridodecylphenyl-perylene-3,4:9,10-tetracarboxylic acid bisimide 
• 130296-43-4 N¹-(3-Cyanphenyl)-N²-(2,5-di-tert-butylphenyl)-3,4:9,10-perylentetracarboxdiimid 
• 130296-44-5 N¹-(4-Aminobutyl)-N²-(2,5-di-tert-butylphenyl)-3,4:9,10-perylentetracarboxdiimid 
• 118561-00-5 N²-(2,5-Di-tert-butylphenyl)-N¹-(2-hydroxyethyl)-3,4:9,10-perylentetracarboxdiimid 
• 130296-49-0 N²-(2,5-Di-tert-butylphenyl)-N¹-ethyl-3,4:9,10-perylentetracarboxdiimid 
• 130296-42-3 N²-(2,5-Di-tert-butylphenyl)-N'-ethyl-3-amino-4,9,10-perylentricarbonsaeure-3,4-lactam-9,10-imid 

Relevant academic research and scientific papers

Synthesis, electrochemical, and spectroscopic properties of soluble perylene monoimide diesters

Perylene derivatives are an important class of n-type semiconductors. With the exceptions of bay-substituted and N-swallow-tail alkyl/tert-butyl substituted derivatives, most perylene diimides are insoluble. The recently reported perylene tetraesters are highly soluble, but are less electron-deficient. In this paper, a series of perylene monoimide diesters have been synthesized, which have good solubility and acceptable electron-accepting property due to the introducing of imide and ester groups in one perylene molecule. Their electrochemical properties and structural ordering were examined by cyclovoltammetry and X-ray diffraction technique, respectively. Their absorption and emission spectra are reported and discussed.