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4,4',4''-((1,3,5-triazine-2,4,6-triyl)tris(azanediyl))tribenzoic acid is a tris-benzene carboxylic acid derivative with the molecular formula C27H18N6O6. 4,4',4''-((1,3,5-triazine-2,4,6-triyl)tris(azanediyl))tribenzoic acid features a triazine core and is known for its role as a linker in the construction of metal-organic frameworks (MOFs). Its unique chemical structure contributes to the development of new materials with significant industrial and scientific applications.

63557-10-8

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  • 4,4',4''-((1,3,5-triazine-2,4,6-triyl)tris(azanediyl))tribenzoic acid

    Cas No: 63557-10-8

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63557-10-8 Usage

Uses

Used in Metal-Organic Frameworks (MOFs) Production:
4,4',4''-((1,3,5-triazine-2,4,6-triyl)tris(azanediyl))tribenzoic acid is used as a linker in the production of metal-organic frameworks (MOFs) for its ability to connect metal ions and organic units. This role is crucial in the formation of MOFs, which are porous materials with high surface areas and tunable structures.
Used in Gas Storage and Separation:
In the Gas Storage and Separation Industry, 4,4',4''-((1,3,5-triazine-2,4,6-triyl)tris(azanediyl))tribenzoic acid is used as a component in MOFs for its potential in gas storage and separation processes. 4,4',4''-((1,3,5-triazine-2,4,6-triyl)tris(azanediyl))tribenzoic acid's ability to form MOFs with specific pore sizes and functionalities allows for selective adsorption and separation of various gases, making it valuable in applications such as air separation, natural gas purification, and carbon capture.
Used in Catalysis:
In the Catalysis Industry, 4,4',4''-((1,3,5-triazine-2,4,6-triyl)tris(azanediyl))tribenzoic acid is used as a component in MOFs for its potential in catalysis. 4,4',4''-((1,3,5-triazine-2,4,6-triyl)tris(azanediyl))tribenzoic acid's ability to form MOFs with well-defined pore structures and active sites enables the development of efficient catalysts for various chemical reactions, including hydrogenation, oxidation, and hydrolysis processes.
Used in Drug Delivery:
In the Pharmaceutical Industry, 4,4',4''-((1,3,5-triazine-2,4,6-triyl)tris(azanediyl))tribenzoic acid is used as a component in MOFs for drug delivery applications. 4,4',4''-((1,3,5-triazine-2,4,6-triyl)tris(azanediyl))tribenzoic acid's ability to form MOFs with tunable pore sizes and surface functionalities allows for the encapsulation and controlled release of therapeutic agents, improving drug efficacy and reducing side effects.
Overall, 4,4',4''-((1,3,5-triazine-2,4,6-triyl)tris(azanediyl))tribenzoic acid is a versatile compound with a wide range of applications in various industries, primarily due to its role in the construction of metal-organic frameworks with unique properties and functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 63557-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,5 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63557-10:
(7*6)+(6*3)+(5*5)+(4*5)+(3*7)+(2*1)+(1*0)=128
128 % 10 = 8
So 63557-10-8 is a valid CAS Registry Number.

63557-10-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4',4''-((1,3,5-triazine-2,4,6-triyl)tris(azanediyl))tribenzoic acid

1.2 Other means of identification

Product number -
Other names TATAB

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:63557-10-8 SDS

63557-10-8Downstream Products

63557-10-8Relevant articles and documents

A Double-Walled Thorium-Based Metal-Organic Framework as a Promising Dual-Function Absorbent for Efficiently Capturing Iodine and Dyes

Zhang, Na,Sun, Li-Xian,Xing, Yong-Heng,Bai, Feng-Ying

, p. 5686 - 5695 (2019)

We prepared a rare thorium metal-organic framework (MOF) (Th-TATAB) with a double-walled tetrahedral cage structure and giant unit cell volume of 43 ?513 ?3, which is the largest of all reported thorium-based MOFs to our knowledge. The unique structural character allows the thorium-based MOF to exhibit exceptional adsorption properties toward I2 and dyes with different charges. The experimental results show that in cyclohexane solution the absorption ability of Th-TATAB toward I2 can reach about 750 mg/g, and especially the removal efficiency in cyclohexane solution (0.01 mol/L) can reach 90% in 3 h, which far exceeded that of reported [Zn2(tptc)-(apy)2-x(H2O)x]·H2O (80%, 48 h) and MIL-101-NH2 (90%, 30 h). Furthermore, the simultaneous removal of molecules with different charges is very challenging, while Th-TATAB displays excellent adsorption properties for anionic, neutral, and cationic dyes individually and simultaneously from aqueous solution. The exploration of the adsorption performance of MOF Th-TATAB for iodine in cyclohexane solution and dye contaminants in aqueous solution is of great significance for environmental aspects, which provides a new strategy for opening up the potential applications of thorium-based MOFs and understanding actinides chemistry.

Polybenzimidazole and polybenzimidazole/MoS2 hybrids as an active nitrogen sites: Hydrogen generation application

Dinari, Mohammad,Nabiyan, Afshin,Ensafi, Ali. A.,Jafari-Asl, Mehdi

, p. 100996 - 101005 (2015)

Development of free metal or non-noble-metal catalysts for electrode materials with both excellent activity and high stability is essential for hydrogen production. In this work, nitrogen rich polybenzimidazole (PBI) networks were synthesized through a on

Efficient chemical fixation of CO2from direct air under environment-friendly co-catalyst and solvent-free ambient conditions

Das, Rajesh,Ezhil, Thirumavalavan,Muthukumar, D.,Nagaraja, C. M.,Palakkal, Athulya S.,Pillai, Renjith S.

supporting information, p. 23127 - 23139 (2021/10/25)

The capture and conversion of CO2from direct air into value-added products under mild conditions represents a promising step towards environmental remediation and energy sustainability. Consequently, herein, we report the first example of a Mg(

Synthesis, Spectra, and Theoretical Investigations of 1,3,5-Triazines Compounds as Ultraviolet Rays Absorber Based on Time-Dependent Density Functional Calculations and three-Dimensional Quantitative Structure-Property Relationship

Wang, Xueding,Xu, Yilian,Yang, Lu,Lu, Xiang,Zou, Hao,Yang, Weiqing,Zhang, Yuanyuan,Li, Zicheng,Ma, Menglin

, p. 707 - 723 (2018/05/05)

A series of 1,3,5-triazines were synthesized and their UV absorption properties were tested. The computational chemistry methods were used to construct quantitative structure-property relationship (QSPR), which was used to computer aided design of new 1,3,5-triazines ultraviolet rays absorber compounds. The experimental UV absorption data are in good agreement with those predicted data using the Time-dependent density functional theory (TD-DFT) [B3LYP/6–311 + G(d,p)]. A suitable forecasting model (R > 0.8, P 0.0001) was revealed. Predictive three-dimensional quantitative structure-property relationship (3D-QSPR) model was established using multifit molecular alignment rule of Sybyl program, which conclusion is consistent with the TD-DFT calculation. The exceptional photostability mechanism of such ultraviolet rays absorber compounds was studied and confirmed as principally banked upon their ability to undergo excited-state deactivation via an ultrafast excited-state proton transfer (ESIPT). The intramolecular hydrogen bond (IMHB) of 1,3,5-triazines compounds is the basis for the excited state proton transfer, which was explored by IR spectroscopy, UV spectra, structural and energetic aspects of different conformers and frontier molecular orbitals analysis.

A water stable nanometer complex preparation method and application

-

Paragraph 0036; 0041; 0042, (2017/02/09)

The invention relates to a preparation method and application of a hydrostable nano complex. The preparation method comprises the following steps: dissolving zinc nitrate in water to obtain a zinc nitrate water solution, adding the solution into a dimethy

Microwave-assisted SNAr reaction of 2,4,6-trichloro-1,3,5- triazine for the rapid synthesis of C3-symmetrical polycarboxylate ligands

Karuehanon, Weeranuch,Fanfuenha, Watcharee,Rujiwatra, Apinpus,Pattarawarapan, Mookda

experimental part, p. 3486 - 3489 (2012/08/27)

The microwave-assisted SNAr reaction of 2,4,6-trichloro-1,3,5- triazine with various unprotected amino acids was developed for the synthesis of C3-symmetrical polycarboxylate ligands which can be used as structural directing units in

Complexes of iron(III) and chromium(III) salen and salophen Schiff bases with bridging 1,3,5-triazine derived multidirectional ligands

Koc, Ziya Erdem

experimental part, p. 769 - 775 (2011/10/04)

Figure represented. A new synthetic route for preparing multidirectional ligands was developed by using 2,4,6-trichloro-1,3,5-triazine (cyanuric chloride) as core. The reaction included the selective substitutions of 4-aminobenzoic acid onto three chlorides of the triazine ring via a stepwise manner at 1:1, 1:2, or 1:3 equiv. and 0, 25, 130°C, respectively. An efficient synthesis of a novel class of "multidirectional ligands" has been developed based on high-yielding chloride substitutions of 2,4,6-trichloro-1,3,5-triazine by amines. Sixteen new mono-, di-, tri-, and tetra-nuclear Fe(III) and Cr(III) complexes involving tetradenta Schiff bases N,N′-bis(salicylidene)ethylenediamine-(salenH2) or bis(salicylidene)-o-phenylenediamine-(salophenH2) with two new 1,3,5-triazine derived multidirectional ligands were synthesized and characterized by means of elemental analysis, 1H NMR, FT-IR spectroscopy, LC-MS analysis, AAS, thermal analysis, and magnetic susceptibility measurements. The complexes were also characterized as low-spin distorted octahedral Fe(III) and Cr(III) bridged by carboxylic acids. It was understood that the [{Fe(salen)/(salophen)}2O] and [{Cr(salen)/(salophen)} 2O] containing compounds could be represented by the electronic structure of t2g5eg0 and t 2g3eg0.

An efficient, "green" approach to aryl amination of cyanuric chloride using acetic acid as solvent

Kolmakov, Kirill A.

, p. 533 - 539 (2008/09/18)

(Chemical Equation Presented) Acetic acid is an inexpensive and environmentally friendly solvent for facile, clean and high-yielding aryl amination of cyanuric chloride with aromatic amines, including nitroanilines. Aryl animation in acetic acid medium and isolation protocol are greatly simplified as compared to previously reported procedures. Under proper conditions, it is possible to attach the same or different aniline residues in a controlled way to obtain in excellent yields symmetrical and unsymmetrical 1,3,5-triazine derivatives, respectively.

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