136460-29-2

Upstream product

• 606-21-3 1-chloro-2,6-dinitrobenzene 
• 136460-28-1 3-(2-propenyl)-4-(2-propenyloxy)-2',6'-dinitrobiphenyl 
• 129001-63-4 4-(2-propenyloxy)-2',6'-dinitrobiphenyl 
• 129001-64-5 4-hydroxy-3-(2-propenyl)-2',6'-dinitrobiphenyl 
• 5110-82-7 4-methoxy-2',6'-dinitrobiphenyl 
• 696-62-8 para-iodoanisole 
• 100-39-0 benzyl bromide 
• 129001-65-6 3,5-bis(2-propenyl)-4-hydroxy-2',6'-dinitrobiphenyl 
• 129001-62-3 4-hydroxy-2',6'-dinitrobiphenyl 

Downstream Products

• 129001-67-8 4-(benzyloxy)-3,5-bis(3-bromopropyl)-2',6'-diaminobiphenyl 
• 136460-30-5 4-(benzyloxy)-3,5-bis(3-bromopropyl)-2',6'-dinitrobiphenyl 
• 129001-68-9 4-(benzyloxy)-3,5-bis(3-bromopropyl)-2',6'-bis(6-bromohexanamido)biphenyl 
• 129001-71-4 3,5-bis<3-(2-formyl-3,5-dimethylphenoxy)propyl>-4-hydroxy-2',6'-bis<6-(2-formyl-3,5-dimethylphenoxy)hexanamido>biphenyl 
• 129001-70-3 4-(benzyloxy)-3,5-bis<3-(2-formyl-3,5-dimethylphenoxy)propyl>-2',6'-bis<6-(2-formyl-3,5-dimethylphenoxy)hexanamido>biphenyl 
• 129001-66-7 4-(benzyloxy)-3,5-bis(3-hydroxypropyl)-2',6'-dinitrobiphenyl 

Relevant academic research and scientific papers

Pendant-Capped Porphyrins. 1. the Synthesis of a Biphenyl Pendant-Capped Iron(III) Porphyrin Model of Catalase

A phenol pendant-capped porphyrin ((PHPCP)H2) and its iron(III) complex ((PPCP)FeIII) have been synthesized. C NMR were used to characterize all intermediates leading to the final product. In addition, the heteronuclearH shift correl