267897-49-4

Upstream product

• 255062-85-2 2-octyloxybenzoic acid methyl ester 
• 111-83-1 1-bromo-octane 
• 17302-46-4 methyl 2-hydroxy-5-nitrobenzoate 
• 96-97-9 5-nitrosalicylic acid 
• 119-36-8 methyl salicylate 

Downstream Products

• 267897-52-9 N-((ethoxycarbonyl)methyl)-5-amino-2-(octyloxy)benzamide 
• 267897-50-7 N-((ethoxycarbonyl)methyl)-2-(octyloxy)-5-nitrobenzamide 
• 807631-50-1 (2-octyloxy-5-undec-10-enoylaminobenzoylamino)acetic acid 
• 807631-37-4 (2-octyloxy-5-undec-10-enoylaminobenzoylamino)acetic acid ethyl ester 
• 807631-42-1 C₆₄H₉₈N₄O₇ 
• 13736-66-8 (5-nitro-2-octyloxybenzoylamino)acetic acid 
• 1313405-46-7 C₂₁H₃₁NO₄ 
• 1313405-44-5 C₂₇H₄₃NO₄ 
• 1313405-61-6 C₄₆H₆₄N₄O₁₀ 
• 1313405-42-3 C₄₈H₆₈N₄O₁₀ 
• 1313405-58-1 C₅₀H₇₂N₄O₁₀ 
• 1313405-48-9 C₅₂H₇₆N₄O₁₀ 
• 1313405-34-3 C₅₄H₈₄N₄O₇ 
• 1340541-33-4 C₃₂H₄₈N₄O₅ 

Relevant academic research and scientific papers

Oligoamide duplexes as organogelators

Oligoamide duplexes carrying multiple alkyl side chains were found to serve as gelators for aromatic solvents. The double-stranded backbone was essential for the hierarchical self-assembly of the molecular duplex into fibers of high aspect ratios. The demonstrated gelating abilities may be extended to a large family of analogous H-bonded duplexes having different H-bonding sequences, leading to a unique platform for developing a diverse variety of potential gelators based on a supramolecular and/or a dynamic covalent approach.

Synthesis and single-molecule studies of a well-defined biomimetic modular multidomain polymer using a peptidomimetic β-sheet module

In the pursuit of advanced biomaterials with combined strength, toughness, and elasticity, a new class of well-defined modular polymers has been synthesized, and their nanomechanical properties have been studied using atomic force microscopy. These polymers are based on a peptidomimetic β-sheet-based double-closed loop (DCL) module, which was designed to overcome the limitation of the modular polymers we reported previously (J. Am. Chem. Soc. 2004, 126, 2059). Single-molecule force-extension experiments revealed the sequential unfolding of these modules as the polymer is stretched, resulting in more regular sawtooth-patterned curves similar to those seen in titin and other biopolymers. The single-molecule data agreed well with computer modeling, which suggested that hydrogen bonding and π-stacking are both involved in the formation of small DCL clusters along the polymer chain. Copyright

A highly stable, six-hydrogen-bonded molecular duplex

This paper describes the design, synthesis, and characterization of a hydrogen-bonded molecular duplex (3·4). Two oligoamide molecular strands, 3 and 4, with the complementary hydrogen-bonding sequences ADAADA and DADDAD, respectively, were found to form