528543-96-6

Basic information

• Product Name: 1,3,5-tri(1H-iMidazol-1-yl)benzene
• Synonyms: 1,3,5-tri(1H-iMidazol-1-yl)benzene
• CAS NO: 528543-96-6
• Molecular Formula: C15H12N6
• Molecular Weight: 276.29598
• EINECS: -0
• Mol File: 528543-96-6.mol

Chemical Properties

• Melting Point: 303 °C(dec.)
• Boiling Point: 600.9±50.0 °C(Predicted)
• Appearance: /
• Density: 1.33±0.1 g/cm3(Predicted)
• PKA: 5.71±0.10(Predicted)
• CAS DataBase Reference: 1,3,5-tri(1H-iMidazol-1-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-tri(1H-iMidazol-1-yl)benzene(528543-96-6)
• EPA Substance Registry System: 1,3,5-tri(1H-iMidazol-1-yl)benzene(528543-96-6)

Safety Data

• Hazardous Substances Data: 528543-96-6(Hazardous Substances Data)

Usage

Uses

Used in Material Science:
1,3,5-tri(1H-imidazol-1-yl)benzene is used as a component in creating metal-organic frameworks (MOFs) for their wide range of applications including gas storage, catalysis, and drug delivery. 1,3,5-tri(1H-iMidazol-1-yl)benzene's structure contributes to the formation of these frameworks, which are of significant interest due to their high porosity and tunable properties.
Used in Biological and Medical Research:
1,3,5-tri(1H-imidazol-1-yl)benzene is used as a potential drug carrier in biological and medical research. Its interactions with biological molecules are of interest, as it may enhance the delivery and efficacy of drugs in various therapeutic applications.
Used in Drug Development:
In the pharmaceutical industry, 1,3,5-tri(1H-imidazol-1-yl)benzene is used as a scaffold for the development of new drugs. Its unique chemical properties allow for the design of molecules with specific interactions and activities, potentially leading to the creation of novel therapeutic agents.
Overall, 1,3,5-tri(1H-imidazol-1-yl)benzene's diverse applications across different industries highlight its importance and potential in scientific research and technological advancements.

Upstream product

• 288-32-4 1H-imidazole 
• 626-39-1 1,3,5-trisbromobenzene 

Relevant articles and documents

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Coordination-driven self-assembly of discrete molecular architectures of diverse shapes and sizes has been well studied in the last three decades. Use of dynamic imine bonds for designing analogous metal-free architectures has become a growing challenge r

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Photochromic molecules undergo reversible isomerization upon irradiation with light at different wavelengths, a process that can alter their physical and chemical properties. For instance, dihydropyrene (DHP) is a deep-colored compound that isomerizes to light-brown cyclophanediene (CPD) upon irradiation with visible light. CPD can then isomerize back to DHP upon irradiation with UV light or thermally in the dark. Conversion between DHP and CPD is thought to proceed via a biradical intermediate; bimolecular events involving this unstable intermediate thus result in rapid decomposition and poor cycling performance. Here, we show that the reversible isomerization of DHP can be stabilized upon confinement within a PdII6L4 coordination cage. By protecting this reactive intermediate using the cage, each isomerization reaction proceeds to higher yield, which significantly decreases the fatigue experienced by the system upon repeated photocycling. Although molecular confinement is known to help stabilize reactive species, this effect is not typically employed to protect reactive intermediates and thus improve reaction yields. We envisage that performing reactions under confinement will not only improve the cyclic performance of photochromic molecules, but may also increase the amount of product obtainable from traditionally low-yielding organic reactions.

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