807631-37-4

Upstream product

• 112-38-9 10-undecenoic acid 
• 267897-52-9 N-((ethoxycarbonyl)methyl)-5-amino-2-(octyloxy)benzamide 
• 267897-50-7 N-((ethoxycarbonyl)methyl)-2-(octyloxy)-5-nitrobenzamide 
• 267897-49-4 2-octyloxy-5-nitro-benzoic acid methyl ester 
• 13736-58-8 2-(octyloxy)-5-nitro-benzoic acid 
• 17302-46-4 methyl 2-hydroxy-5-nitrobenzoate 
• 96-97-9 5-nitrosalicylic acid 

Downstream Products

• 1313405-27-4 C₆₆H₉₈N₆O₁₄ 
• 1340541-30-1 C₄₄H₆₆N₄O₁₁ 
• 1313405-23-0 C₅₀H₇₆N₄O₈ 
• 807631-42-1 C₆₄H₉₈N₄O₇ 
• 807631-50-1 (2-octyloxy-5-undec-10-enoylaminobenzoylamino)acetic acid 

Relevant academic research and scientific papers

Interplay of olefin metathesis and multiple hydrogen bonding interactions: Covalently cross-linked zippers

Hydrogen-bonded zippers bearing terminal alkene groups were treated with Grubbs' catalyst, leading to covalently cross-linked zippers without violating H-bonding sequence specificity. The yield of a cross-linked zipper depended on the stability of its H-b

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