35122-97-5

Upstream product

• 32315-10-9 bis(trichloromethyl) carbonate 
• 626-40-4 3,5-dibromoaniline 
• 618-58-6 3,5-dibromobenzoic acid 
• 75-44-5 phosgene 

Downstream Products

• 1566-99-0 C₁₅H₁₂Br₂N₂O₃ 
• 1449294-69-2 3-(3,5-dibromophenyl)-2,4(1H,3H)-quinazolinedione 
• 103277-06-1 8,17-dioxo-2,7,18,23-tetraoxa-9,16-diaza-tetracosanedioic acid bis-(3,5-dibromo-anilide) 
• 83015-05-8 (3,5-dibromo-phenyl)-carbamic acid ethyl ester 

Relevant academic research and scientific papers

Effective Synthesis and Modification of α-Cyclodextrin-Based [3]Rotaxanes Enabling Versatile Molecular Design

One-pot synthesis of various α-cyclodextrin-(α-CD-) based [3]rotaxanes in water and their structural modifications are discussed in detail. Pseudo[3]rotaxane was prepared from α-CD and α,ω-diaminododecane in water (above 100 g, quantitative yield in a 1 L

Specific inhibitors of puromycin-sensitive aminopeptidase with a 3-(halogenated phenyl)-2,4(1H,3H)-quinazolinedione skeleton

Specific puromycin-sensitive aminopeptidase (PSA) inhibitors with a 3-(halogenated phenyl)-2,4(1H,3H)-quinazolinedione skeleton were prepared and their structure-activity relationships were investigated. The nature (F, Cl or Br), number and position(s) of the halogen atom(s) introduced into the 3-phenyl group were concluded to be critical determinants of the inhibitory activity.