108480-48-4

Upstream product

• 824-45-3 2,5-dimethylbenzyl chloride 
• 952303-55-8 (4-bromo-2,5-dimethylphenyl)methanol 
• 1074-24-4 2,5-dibromo-p-xylene 
• 88111-74-4 bromo-4 dimethyl-2,5 benzaldehyde 

Downstream Products

• 88111-74-4 bromo-4 dimethyl-2,5 benzaldehyde 
• 854693-42-8 4-bromo-2,5-dimethyl-3,6-dinitro-benzyl chloride 
• 952303-56-9 2-(4-bromo-2,5-dimethylbenzyl)malonic acid diethyl ester 
• 900027-21-6 3-(4-bromo-2,5-dimethylphenyl)propionic acid 
• 952303-57-0 6-bromo-4,7-dimethylindan-1-one 
• 952303-63-8 C₁₈H₁₆N₄O 
• 519-23-3 ellipticine 
• 10371-86-5 9-methoxyellipticine 
• 109855-79-0 7-(2-azidophenyl)-5,8-dimethylisoquinoline 
• 1170667-43-2 4-bromo-2,5-dimethylbenzyldiethylphosphonate 
• 854693-40-6 4-bromo-2,5-dimethyl-3,6-dinitro-benzyl iodide 
• 276677-03-3 4-bromo-2,5-dimethylbenzoic acid 

Relevant academic research and scientific papers

Supramolecular assembly of H-bonded copolymers/complexes/nanocomposites and fluorescence quenching effects of surface-modified gold nanoparticles on fluorescent copolymers containing pyridyl H-acceptors and acid H-donors

A series of photoluminescent (PL) and liquid crystalline (LC) self-H-bonded side-chain copolymers (P1-P3) consisting of pyridyl H-acceptors and isomeric acid H-donors (i.e., para-, meta-, and ortho-benzoic acids) were synthesized. Supramolecular H-bonded

Preparation of polyfunctional aryl azides from aryl triazenes. A new synthesis of ellipticine, 9-methoxyellipticine, isoellipticine, and 7-carbethoxyisoellipticine

(Chemical Equation Presented) The preparation of polyfunctional aryl azides by the reaction of aryl triazenes with NaN3 in the presence of KHSO4 or BF3·OEt2/TFA (trifluoroacetic acid) has been described. A variety of functional groups (halides, esters, ketones, nitriles, aldehydes, and boronic esters) are tolerated under the Lewis acidic conditions. By using this methodology, the potent antitumor agents, ellipticine and 9-methoxyellipticine, have been synthesized. In addition, isoellipticine and a related derivative, 7-carbethoxyisoellipticine, were also prepared.