59827-85-9

Usage

Uses

Used in Scientific Research:
1H-Isoindole-1,3(2H)-dione, 5-amino-6-nitrois used as a research compound for [application reason] in the field of chemistry and materials science. Its unique chemical properties make it a valuable tool for studying various chemical reactions and processes. 1H-Isoindole-1,3(2H)-dione, 5-amino-6-nitro-'s structure and reactivity can provide insights into the behavior of similar compounds and contribute to the development of new materials and applications.

Upstream product

• 7147-90-2 4-chlorophthalimide 
• 3676-85-5 4-aminophthalimide 
• 136918-14-4 phthalimide 
• 89-40-7 4-nitrophthalimide 
• 6015-57-2 5-chloro-6-nitroisoindole-1,3-dione 

Downstream Products

• 1008449-77-1 5-amino-2-(1-methyl-piperidin-4-yl)-6-nitro-isoindole-1,3-dione 
• 1008449-78-2 5-Amino-2-[2-(1H-imidazol-4-yl)-ethyl]-6-nitro-isoindole-1,3-dione 
• 1008449-92-0 5-Amino-2-[2-(4-methyl-piperazin-1-yl)-ethyl]-6-nitro-isoindole-1,3-dione 
• 1188412-95-4 5-amino-2-(2-(dimethylamino)ethyl)-6-nitroisoindoline-1,3-dione 
• 1008452-51-4 5-Amino-6-nitro-2-(2-pyrrolidin-1-ylethyl)-1H-isoindole-1,3(2H)-dione 
• 1397682-07-3 5,6-diamino-2-dodecylisoindoline-1,3-dione 
• 1403965-06-9 6-dodecyl-4,8-bis(5-bromothiophen-2-yl)pyrrolo[3,4-f]-2,1,3-benzothiadiazole-5,7-dione 
• 1397682-04-0 6-dodecyl-5H-[1,2,5]thiadiazolo[3,4-f]isoindole-5,7(6H)-dione 
• 59673-89-1 5,6-diamino-2,3-dihydro-1H-isoindole-1,3-dione 
• 1008459-97-9 C₂₁H₂₀ClN₅O₃*ClH 
• 1008449-07-7 C₂₂H₂₂ClN₅O₃ 
• 1008451-65-7 C₁₇H₁₂BrClN₄O₃ 
• 1008451-63-5 C₁₀H₁₀BrN₃O₂ 

Relevant academic research and scientific papers

Novel n-channel organic semiconductor based on pyrene-phenazine fused monoimide and bisimides

Large π-conjugated pyrene-phenazine monoimide and bisimides were synthesized by imine condensation reaction. These imides form well ordered 1D nanotapes upon self-assembly in solution. Electrochemical and electric conductivity measurement reveal it can be served as an n-channel semiconductor with large charge carrier mobility up to 4.1 cm2 V?1 s?1. Both alkylated imides are highly luminescent, and can be quenched via protonization using trifluoroacetic acid, which could be served as potential colorimetric acid sensors.

Tricyclic compound derivatives useful in the treatment of neoplastic diseases, inflammatory disorders and immunomodulatory disorders

Provided are compounds of the formula (I): or a stereoisomer, tautomer, salt, hydrate or prodrug thereof that modulate tyrosine kinase activity, compositions comprising the compounds and methods of their use.