102890-87-9

Upstream product

• 620-24-6 3-Hydroxybenzyl alcohol 
• 4101-68-2 1,10-dibromodecane 

Downstream Products

• 651300-09-3 1,10-bis{3-[4-ethoxycarbonyl-2-(3-methyl-2-nitrophenyl)benzimidazol-1-ylmethyl]phenoxy}decane 
• 651300-18-4 1,10-bis{3-[4-ethoxycarbonyl-2-(3-methyl-2-aminophenyl)benzimidazol-1-ylmethyl]phenoxy}decane 
• 651299-87-5 1,10-bis{3-[2-(2-amino-3-methylphenyl)-4-hydroxycarbonylbenzimidazol-1-ylmethyl]phenoxy}decane 
• 560086-38-6 1,10-bis{3-[4-ethoxycarbonyl-2-(2-nitrophenyl)benzimidazol-1-ylmethyl]phenoxy}decane 
• 560086-42-2 1,10-bis{3-[2-(2-aminophenyl)-4-ethoxycarbonylbenzimidazol-1-ylmethyl]phenoxy}decane 
• 560086-46-6 1,10-bis{3-[2-(2-aminophenyl)-4-hydroxycarbonylbenzimidazol-1-ylmethyl]phenoxy}decane 
• 560086-34-2 1,10-bis(3-bromomethylphenoxy)decane 

Relevant academic research and scientific papers

Ruffling-Induced Chirality: Synthesis, Metalation, and Optical Resolution of Highly Nonplanar, Cyclic, Benzimidazole-Based Ligands

Expedient five-step syntheses of a cyclic bis(benzimidazole)-based amide 5 and two sterically more hindered analogues 23-24 have been developed. These amides are chiral due to the inherent ruffling of the macrocyclic plane. Racemization of the optical ant