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Usage

Uses

Used in Pharmaceutical Industry:
4,4′-(4-amino-1,2,4-triazol-3,5-diyl)dibenzoic acid is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique structure and properties make it a valuable building block in the development of new pharmaceutical compounds.
Used in Antimicrobial Applications:
4,4′-(4-amino-1,2,4-triazol-3,5-diyl)dibenzoic acid is used as an antimicrobial agent due to its biological activity against various microorganisms. Its ability to inhibit the growth of bacteria and fungi makes it a promising candidate for use in antimicrobial formulations and treatments.
Used in Antifungal Applications:
4,4′-(4-amino-1,2,4-triazol-3,5-diyl)dibenzoic acid is used as an antifungal agent for its potential to combat fungal infections. Its effectiveness against fungi highlights its potential use in antifungal medications and treatments.
Used in Material Science:
4,4′-(4-amino-1,2,4-triazol-3,5-diyl)dibenzoic acid is used in the development of new materials due to its unique chemical structure and properties. It may serve as a building block for the synthesis of other organic compounds or be incorporated into materials with specific characteristics for various applications.
Used in Chemical Research:
4,4′-(4-amino-1,2,4-triazol-3,5-diyl)dibenzoic acid is used as a subject of interest in chemical research. Its structure and properties make it a valuable compound for studying various chemical reactions and processes, contributing to the advancement of chemical knowledge and technology.

Upstream product

• 619-65-8 4-cyanobenzoic Acid 

Relevant academic research and scientific papers

The substituent effect on the luminescent properties of a set of 4-amino-4H-1,2,4-triazole: Syntheses, crystal structures and Hirshfeld analyses

A set of compounds based on 4-amino-4H-1,2,4-triazole group, namely, 4,4′-(4-amino-4H-1,2,4-triazole-3,5-diyl)dibenzoic acid (1), 4,4′-(4-amino-4H-1,2,4-triazole-3,5-diyl)dianiline (2), 4,4′-(4-amino-4H-1,2,4-triazole-3,5-diyl)diphenol (3), were obtained

Crystallographic Visualization of Postsynthetic Nickel Clusters into Metal-Organic Framework

Postsynthetic metalation (PSM) has been employed as a robust method for the postsynthetic modification of metal-organic frameworks (MOFs). However, the lack of relevant information that can be obtained for the postsynthetically introduced metallic ions has hindered the development of PSM applications. Thanks to the advancement in single-crystal X-ray diffraction (SCXRD) technology, there have been a few recent examples in which successful postsynthetic introduction of single metal ions into MOFs occurred at the defined chelating sites. These works have provided useful explanations about the complicated host-guest chemistry involved in PSMs. On the other hand, there are only limited examples with crystallographic snapshots of the postsynthetic installation of metal clusters into the pores of MOFs using an ordinary SCXRD due to the loss of crystallinity of parent matrix during the PSM process. Herein, by the careful selection of starting materials and controlling the reaction conditions, we report the first crystallographic visualization of metal clusters inserted into Zr-based MOFs via PSM. The structural advantages of the parent Zr-MOF, which are inherited from the stable Zr6 cluster and triazole-containing dicarboxylate ligand, ensure both the preservation of high crystallinity and the presence of flexible coordination sites for PSM. Furthermore, PSM of metal clusters in a MOF pore space enhances stability of the final samples while also imparting the functionality of a successful catalyst toward ethylene dimerization reaction. The related construction ideas and structural information detailed in this work can help lay the foundation for further advancements using the postmodification of MOFs as well as open new doors for the utilization of SCXRD technology in the field of MOFs.