81882-78-2

Upstream product

• 34240-09-0 3-(benzyloxycarbonylamino)benzoic acid 
• 99-05-8 meta-aminobenzoic acid 
• 39887-56-4 3-nitro-N-propylbenzamide 
• 121-90-4 m-nitrobenzoic acid chloride 
• 148582-25-6 3-(((benzyloxy)carbonyl)amino)benzoyl chloride 

Downstream Products

• 1001426-41-0 C₁₃H₁₇BrN₂O₂ 
• 1156201-81-8 3-(2-chloroacetamido)-N-propylbenzamide 
• 1263056-13-8 C₃₄H₃₁N₄O₂⁽¹⁺⁾*Cl^(1-) 

Relevant academic research and scientific papers

Synthesis and anion recognition studies of new oligomethylene bis(nitrophenylureylbenzamide) receptors

A new series of oligomethylene bis(nitrophenylureylbenzamide) receptors were synthesized varying the relative position of the urea and amide groups (ortho4 and meta8) and the length of the oligomethylene chain (C2 to C8). An anion re

2,4-Pyrimidinediamine Compounds and Their Uses

The present invention provides 2,4-pyrimidinediamine compounds that inhibit the IgE and/or IgG receptor signaling cascades that lead to the release of chemical mediators, intermediates and methods of synthesizing the compounds and methods of using the compounds in a variety of contexts, including in the treatment and prevention of diseases characterized by, caused by or associated with the release of chemical mediators via degranulation and other processes effected by activation of the IgE and/or IgG receptor signaling cascades.

Benzimidazolium-based receptors: Case of iodide-water cluster induced supramolecular chain and improved fluorometric binding of iodide involving alcoholic group

Benzimidazolium-based receptors 1 and 2 have been designed and synthesized. Anion binding studies reveal their selective fluorescence sensing of iodide in the excited state by exhibiting greater quenching of emission of anthracene. In the ground state, they prefer to bind bromide ion. Incorporation of alcoholic -OH in 2 leads to better performance over the receptor 1. The cyclooctameric structure as constituted by inclusion water and iodide interaction leads to ID-supramolecular chain with the structure 1 in the solid state. 1H NMR, UV-vis and fluorescence spectroscopic methods were adopted to study the anion binding behavior.

A new benzimidazolium receptor for fluorescence sensing of iodide

A new anthracene-appended benzimidazolium-based receptor 1 has been designed and synthesised. The receptor shows selective recognition of iodide in the excited state by exhibiting quenching of emission of anthracene. In the ground state, receptor 1 shows

3-(2′-Bromopropionylamino)-benzamides as novel S-phase arrest agents

We report the synthesis, antiproliferative activity, and SAR of novel 3-(2′-bromopropionylamino)-benzamides. Many of the benzamide compounds showed potent cytotoxicities against Molt-3 leukemia cells. Several compounds exihibited cytotoxicities (under 6.5

Thermosensitive recording material and novel color developer compounds

Disclosed is a thermosensitive recording material comprising a sheet-shaped support and a thermosensitive recording layer which is formed on at least one surface of the support and comprises a colorless or light-colored dye precursor and a color developer capable of reacting with the dye precursor and inducing color formation therein upon application of heat thereto, the color developer comprising a compound represented by the following formula (I) or analog thereof:: The thermosensitive recording material has high sensitivity and can prevent white background portions from coloring and recorded images from decolorizing in an environmental resistance test.

Convergent functional groups. 13. High-affinity complexation of adenosine derivatives within induced binding pockets

Receptors based upon 3,6-diaminocarbazole have been synthesized that bind to adenosine derivatives with an interaction energy of approximately 8 kcal/mol in CDCl3 and over 3 kcal/mol in CD3OD. The purine nucleus is bound within a cavity by simultaneous Watson-Crick and Hoogsteen base-pairing, hydrogen bonding to N3, and stacking on both of its aromatic faces. Hydrogen bond interactions can be estimated at approximately 0.5-0.75 kcal/mol in methanol. The structure of the complex in solution has been deduced through binding assays of incremental derivatives, one- and two-dimensional NMR studies, and molecular modeling.