264270-90-8

Upstream product

• 6066-82-6 1-hydroxy-pyrrolidine-2,5-dione 
• 1679-64-7 Monomethyl terephthalate 
• 1571-08-0 methyl 4-formylbenzoate 
• 6908-41-4 4-(methoxycarbonyl)benzyl alcohol 

Downstream Products

• 195305-15-8 N,N'-bis-(4-carboxybenzoyl)-1,4-butanediamine 
• 40872-99-9 N,N'-bis-(4-carboxybenzoyl)-1,2-ethanediamine 
• 128439-62-3 N,N'-bis-(4-carboxybenzoyl)-1,3-propanediamine 
• 7060-10-8 N,N'-bis-(4-methoxycarbonylbenzoyl)-1,2-ethanediamine 
• 102810-33-3 N,N'-bis-(4-methoxycarbonylbenzoyl)-1,4-butanediamine 
• 1414944-12-9 N,N',N''-tris-(4-methoxycarbonylbenzoyl)-tris-(2-aminoethyl)amine 
• 1515864-99-9 C₅₁H₇₇NO₃₇ 
• 1452840-74-2 5'-O-[N-(4-carboxylatobenzoyl)sulfamoyl]cytidine sodium salt 
• 1452840-73-1 5'-O-[N-(4-methoxycarbonylbenzoyl)sulfamoyl]cytidine 

Relevant academic research and scientific papers

Interfacial and Nanoconfinement Effects Decrease the Excited-State Acidity of Polymer-Bound Photoacids

Photo-initiated ion transport on the nanoscale is relevant to various fields including energy conversion, neuron triggering, and biomimetic processes. To study this phenomenon, we synthesized and evaluated photoacid-modified polymers, which generate hydra

Selection between pinching-type and supramolecular polymer-type complexes by α-cyclodextrin-β-cyclodextrin hetero-dimer and hetero-cinnamamide guest dimers

Novel supramolecular complexes have been prepared from an α-cyclodextrin-β-cyclodextrin heterodimer (α-CD-β-CD hetero-dimer) and hetero-cinnamamide guest dimers, G-t-Boc and G-NH2, having adamantyl groups in aqueous solutions. On addition of th

Metal-free intermolecular C-O cross-coupling reactions: Synthesis of: N -hydroxyimide esters

Selectfluor-mediated intermolecular C-O cross coupling reaction for the synthesis of N-hydroxyimide esters was developed for the first time. The reaction is applicable to the coupling of readily available aryl and alkyl aldehydes with N-hydroxyphthalimide (NHPI) and N-hydroxysuccinimide (NHSI). The resulting active esters can be directly converted into amides in one pot.

Functional materials from the covalent modification of reduced graphene oxide and β-cyclodextrin as a drug delivery carrier

We report a drug delivery system based on the covalently reduced graphene oxide (rGO) with p-aminobenzoic acid (rGO-C6H4-COOH) for the loading and targeted delivery of the anticancer drug, doxorubicin (DOX). The colloidal solution of

Sialyltransferase inhibitors: Consideration of molecular shape and charge/hydrophobic interactions

In order to evaluate the importance of molecular shape of inhibitor molecules and the charge/H-bond and hydrophobic interactions, we synthesized three types of molecules and tested them against a sialyltransferase. The first type of compounds were designe

Synthesis and characterization of bis-and tris-(4-carboxybenzoyl)- alkaneamines

A practical and efficient protocol to obtain bis- and tris-(4- carboxybenzoyl)alkaneamines based on monoprotected 1,4-benzenedicarboxylic acid is reported here. N-(4-methoxycarbonylbenzoyloxy)succinimide was treated with aliphatic diamines and triamines to form aliphatic hydrocarbon-linked bis- and tris-amides 4a-4e. The yields ranged from good to very good and showed that choosing the right acylating agent is a key point in this synthesis. All the compounds were characterized by elemental analysis, FTIR, and 1H NMR.

N-hydroxysuccinimide-promoted oxidation of primary alcohols and aldehydes to form active esters with hypervalent(III) iodine

A simple, mild, and efficient method for the conversion of primary alcohols and aldehydes to N-hydroxysuccinimide esters with (diacetoxyiodo)benzene in high yield is developed. N-Hydroxysuccinimide acts not only as an esterification partner but also as an activator of PhI(OAc)2 in this reaction. Copyright