1327339-67-2

Upstream product

• 3132-99-8 m-bromobenzoic aldehyde 
• 75-52-5 nitromethane 
• 29816-74-8 3-(3-bromophenyl)-1-phenylprop-2-en-1-one 
• 98-86-2 acetophenone 
• 115665-95-7 3-bromo-β-nitro-styrene 
• 120-46-7 1,3-diphenylpropanedione 

Downstream Products

• 1327339-69-4 [3-(3-bromophenyl)-5-phenyl-1H-pyrrol-2-yl][3-(3-bromophenyl)-5-phenylpyrrol-2-ylidene]amine 
• 1327339-72-9 C₃₂H₂₀BBr₂F₂N₃ 
• 1255378-04-1 3-(3-bromo-phenyl)quinolin-2(1H)-one 

Relevant academic research and scientific papers

Sequential Michael addition/retro-Claisen condensation of 1,3-diarylpropan-1,3-diones with nitrostyrenes: one-step synthesis of 4-nitro-1,3-diarylbutan-1-ones

Abstract : The sequential Michael addition/retro-Claisen condensation of 1,3-diarylpropan-1,3-diones with nitrostyrenes is described. 4-Nitro-1,3-diarylbutan-1-ones were efficiently synthesized in good to high yield under mild, transition-metal-free condition. This one-step method involving sequential carbon-carbon bond formation and cleavage provides a good alternative to the synthesis of various γ-nitro ketones. Graphical abstract: The sequential Michael addition/retro-Claisen condensation of 1,3-diarylpropan-1,3-diones with nitrostyrenes is described. 4-Nitro-1,3-diarylbutan-1-ones were efficiently synthesized in good to high yield under mild and transition-metal-free condition. [Figure not available: see fulltext.].

Synthesis of Aza-BODIPY boron difluoride PDT agents to promote apoptosis in HeLa cells

BF2 Chelated azadipyrromethene dyes fluoresce in the near infrared and have potential applications in photodynamic therapy. When irradiated above 600nm these aza-BODIPY compounds react with triplet O 2 in the body to form a reactive