768377-92-0

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 98-86-2 acetophenone 
• 959-33-1 3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one 

Downstream Products

• 1016989-94-8 [(3-(4-methoxyphenyl)-5-phenyl-1H-pyrrol-2-yl)(3-(4-methoxyphenyl)-5-phenylpyrrol-2-ylidene)amine]zinc 
• 1186317-59-8 (triphenylphosphine)Ag(N(C₄HN(C₆H₅)C₆H₄OCH₃)2) 
• 1186317-63-4 (triethylphosphine)Ag(N(C₄HN(C₆H₅)C₆H₄OCH₃)2) 
• 1186317-55-4 (triphenylphosphine)Cu(N(C₄HN(C₆H₅)C₆H₄OCH₃)2) 
• 850006-86-9 C₃₄H₂₅Br₂N₃O₂ 

Relevant academic research and scientific papers

In vitro photodynamic treatment of cancer cells induced by aza-BODIPYs

Two aza-BODIPY photosensitizers (PSs, compounds 7 and 8), featuring an iodine atom on each pyrrolic unit of their structure, were synthesized in fairly good yields starting from commercial products and tested in vitro on two human cancer cell lines (HCT11

Gold(I) complexes of brominated azadipyrromethene ligands

Azadipyrromethenes are luminescent, red-light absorbing dyes that readily bind BF2+ and metals. Their framework allows for structural modification at the phenyl arms and the two pyrrolic carbon positions. Here we report five new gold

Synthesis, optical properties and ultrafast dynamics of aza-boron-dipyrromethene compounds containing methoxy and hydroxy groups and two-photon absorption cross-section

In this work, aza-boron-dipyrromethene (aza-BODIPY) compounds containing methoxy and hydroxy groups were synthesized. The effects of substitution and intramolecular charge transfer on linear and nonlinear optical absorptions (especially two photon absorpt