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Tris(2-(2-nitrophenoxy)ethyl)amine, also known as TNEA, is a chemical compound with the molecular formula C18H22N2O6. It is a tris-derivative of ethylenediamine, where each nitrogen atom is connected to a 2-(2-nitrophenoxy)ethyl group. TNEA is a yellow crystalline solid that is soluble in water and organic solvents. It is used as a chelating agent, particularly for metal ions such as copper, iron, and zinc, and has applications in various fields, including analytical chemistry, pharmaceuticals, and materials science. Due to its ability to form stable complexes with metal ions, TNEA can be employed in the synthesis of metal-organic frameworks and as a stabilizer in certain chemical reactions.

74145-47-4

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74145-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74145-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,4 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74145-47:
(7*7)+(6*4)+(5*1)+(4*4)+(3*5)+(2*4)+(1*7)=124
124 % 10 = 4
So 74145-47-4 is a valid CAS Registry Number.

74145-47-4Relevant academic research and scientific papers

Binding of HgCl2 by a nitro functionalized tripodal receptor and its decomplexation controlled by anion complexation

Dey, Sandeep Kumar,Das, Gopal

experimental part, p. 429 - 438 (2011/05/07)

The presence of a nitro functionality on N-bridged tripodal receptors has an effect on its binding ability towards HgCl2 by coordination through one of the nitro oxygen atoms, ethereal oxygen and the bridgehead nitrogen atom. Decomplexation of HgCl2 and recovery of the receptor L can be accomplished by the formation of anion complexes with [L·HgCl2]. The complexation of different anions with multiple protonated receptor units is attributable to intramolecular (N-H) +·A·A·on interactions, at the same time the presence of multiple C- HA·A·A·anion and interligand C-H·A·A·Onitro hydrogen bonds provide added stabilization. Protonation at the bridgehead nitrogen atom and the presence of the nitro functionality render the aliphatic and aryl protons sufficiently acidic for their active participation in moderate to weak C-H·A·A·anion and C- H·A·A·Onitro interactions. Spectroscopic studies provide evidence for the formation of anion complexes from [LA·HgCl2] by extrusion of HgCl2. The strategic use of anion binding as a driving force for the templated assembly of the tripodal ligand L has been accomplished by the reversible complexationand decomplexation of [LA·HgCl2] extruding HgCl2 by employing mildly acidic ammonium salts. Copyright

Tripod-like compounds: Syntheses of tris(p- or o-amino phenoxymethyl)-propane, tris(p- or o-amino phenoxyethyl)amine, and their schiff base or salicyl derivatives

Lu,Fan,Zhao,Wu

, p. 1531 - 1540 (2007/10/03)

Tris(nitrophenoxymethyl)propane and tris(nitrophenoxyethyl)amine, prepared by the reaction of trimethylol propane or triethanol amine with p- or o-chloronitrobenzene, were reduced to give the corresponding amines. The amines condensed with 2-pyridinecarboxaldehyde, 2-quinoline-carboxaldehyde, or salicylaldehyde to give the tripod Schiff bases. The tripodal salicylamides were obtained by condensation of salicylic acid with the amines in the presence of phosphorus trichloride.

Ligand Structure and Complexation, LI. - Multidentate Neutral Ligands with Variable Cavities and Pseudo Cavities

Sieger, Heinz,Voegtle, Fritz

, p. 425 - 440 (2007/10/02)

New cyclic and non-cyclic neutral ligand systems have been synthesized.They contain repeating oligoethylene glycol ethers and carboxamide functions, which allow attractive interactions between single chain segments and with terminal groups.Crystalline com

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