70752-22-6

Upstream product

• 81574-75-6 2,4-dimethoxy-5-nitro-benzoic acid methyl ester 

Downstream Products

• 914939-29-0 5-(2-tert-butoxycarbonylamino-2-methyl-propionylamino)-2,4-dimethoxy-benzoic acid methyl ester 
• 915184-68-8 methyl 5-(2,4-diisobutoxy-5-nitrobenzoylamino)-2,4-dimethoxybenzoate 
• 956108-82-0 5-(2,4-dimethoxy-benzylamino)-2,4-dimethoxy-benzoic acid methyl ester 
• 915184-70-2 5-[(2,4-diisobutoxy-5-nitro-benzoyl)-(2,4-dimethoxybenzyl)-amino]-2,4-dimethoxybenzoic acid 
• 915184-67-7 5-[(2,4-diisobutoxy-5-nitro-benzoyl)-(2,4-dimethoxy-benzyl)-amino]-2,4-dimethoxy-benzoic acid methyl ester 
• 915184-69-9 methyl 5-[5-(2,4-dimethoxy-benzylamino)-2,4-diisobutoxy-benzoylamino]-2,4-dimethoxybenzoate 
• 915184-72-4 5-[(5-{5-[(2,4-diisobutoxy-5-nitro-benzoyl)-(2,4-dimethoxy-benzyl)-amino]-2,4-dimethoxy-benzoylamino}-2,4-diisobutoxy-benzoyl)-(2,4-dimethoxy-benzyl)-amino]-2,4-dimethoxy-benzoic acid methyl ester 
• 915184-73-5 5-[(5-{5-[(2,4-diisobutoxy-5-nitro-benzoyl)-(2,4-dimethoxy-benzyl)-amino]-2,4-dimethoxy-benzoylamino}-2,4-diisobutoxy-benzoyl)-(2,4-dimethoxy-benzyl)-amino]-2,4-dimethoxy-benzoic acid 
• 1383808-72-7 C₇₀H₉₅N₅O₃₀ 
• 1383808-71-6 C₁₀₆H₁₆₇N₅O₁₈ 

Relevant academic research and scientific papers

Multiturn Hollow Helices: Synthesis and Folding of Long Aromatic Oligoamides

Aromatic oligoamides adopting helical conformations are synthesized by coupling carboxyl-terminated basic units having two, four, and eight residues to amine-terminated oligomer precursors. Coupling yields show no noticeable reduction with the size of the

Hydrogen bonding-mediated foldamer-bridged zinc porphyrin-C60 dyads: ideal face-to-face orientation and tunable donor-acceptor interacion

Four porphyrin-bridge-C60 dyads have been synthesized by covalently linking the chromophores at the opposite ends of a hydrogen bonded arylamide-derived foldamer bridge. For comparison, four C60-free porphyrin derivatives of the same frameworks have also been prepared. The fully hydrogen bonded bridges enable the appended porphyrin and C60 moieties to contact in a face-to-face manner. 1H NMR, UV-vis and fluorescent investigations in chloroform indicate that such a structural matching remarkably facilitates the intramolecular energy and electron transfer and charge separation between the two chromophores and also retards the recombination of the charge-separated state. Removing one hydrogen bond considerably reduces the energy and electron transfer. Further removing another one leads to no important interaction between the chromophores to occur.

Aromatic oligoamide macrocycles from the bimolecular coupling of folded oligomeric precursors

Aromatic oligoamide macrocycles consisting of six to ten meta-linked residues were prepared based on bimolecular coupling/cyclization of a pentameric diamine and oligomeric diacid chlorides, and adopt folded conformations enforced by intramolecular three-

Improving foldamer synthesis through protecting group induced unfolding of aromatic oligoamides

(Chemical Equation Presented) The hydrogen bond rigidified backbones of aromatic oligoamides are temporarily interrupted by replacing the amide hydrogens with the acid-labile 2,4-dimethoxybenzyl (DMB) group, which allows the efficient preparation of long

N-(3-pyrrolidinyl) benzamide derivative

N-(3-Pyrrodinyl)benzamide derivatives represented by the following general formula (I) which have potent and selective antagonism against dopamine D3 and/or D4 receptor and are useful as a psychotropic, a schizophrenia-treating agent and the like, or a pharmaceutically acceptable salt thereof or a pharmaceutical preparation thereof. STR1