56643-83-5

Basic information

• Product Name: 1,4-Bis(imidazole-l-ylmethyl)benzene
• Synonyms: 1,4-Bis(imidazole-l-ylmethyl)benzene;1,4-Bis[(1H-iMidazol-1-yl)Methyl]benzene;1,4-Bis[(1H-imidazol-1-yl)methyl]benzene
• CAS NO: 56643-83-5
• Molecular Formula: C₁₄H₁₄N₄
• Molecular Weight: 238.293
• Product Categories: API intermediates
• Mol File: 56643-83-5.mol
• Article Data: 29

Chemical Properties

• Melting Point: 130.0 to 134.0 °C
• Boiling Point: 487.0±25.0 °C(Predicted)
• Appearance: /
• Density: 1.17±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• Solubility: soluble in Methanol
• PKA: 7.05±0.10(Predicted)
• CAS DataBase Reference: 1,4-Bis(imidazole-l-ylmethyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Bis(imidazole-l-ylmethyl)benzene(56643-83-5)
• EPA Substance Registry System: 1,4-Bis(imidazole-l-ylmethyl)benzene(56643-83-5)

Safety Data

• Hazardous Substances Data: 56643-83-5(Hazardous Substances Data)

Usage

General Description

1,4-Bis(imidazole-1-ylmethyl)benzene, also known as bibenzyl, is a chemical compound with the molecular formula C18H20N4. It is an organic compound that consists of a central benzene ring with two imidazole groups attached to it at the 1 and 4 positions. Bibenzyl has been studied for its potential applications in coordination chemistry, specifically for its ability to form metal complexes. It is also of interest in supramolecular chemistry for its potential as a building block in the construction of complex molecular structures. Bibenzyl may also have potential applications in biological systems, although further research is needed to fully understand its properties and potential uses.

Upstream product

• 288-32-4 1H-imidazole 
• 623-25-6 p-Xylylene dichloride 
• 104-81-4 4-Methylbenzyl bromide 
• 106-42-3 para-xylene 
• 623-24-5 1,4-bis(bromomethyl)benzene 

Downstream Products

• 945223-39-2 C₃₆H₃₂N₈⁽²⁺⁾ 
• 1240519-04-3 poly[[μ2-1,4-bis(imidazol-1-ylmethyl)benzene](μ2-naphthalene-1,4-dicarboxylato)zinc(II)] 
• 1201845-74-0 [Zn(5-bromoisophthalate)(1,4-bis(imidazol-1-ylmethyl)benzene)]_n 
• 1370618-27-1 C₂₀H₂₆N₄O₆S₂ 

Relevant articles and documents

A catalytic approach of blending CO2-activating MOF struts for cycloaddition reaction in a helically interlaced Cu(II) amino acid imidazolate framework: DFT-corroborated investigation

In CO2 transformation catalysis, the synthesis of cyclic carbonates using two classes of MOF catalysts viz., zeolitic imidazolate frameworks (ZIF) and MOFs with carboxylate-capped SBUs have gained large attention. Herein we propose the strategy

The vital role of ditopic: N - N bridging ligands with different lengths in the formation of new binuclear dioxomolybdenum(vi) complexes: Synthesis, crystal structures, supramolecular framework and protein binding studies

A new series of binuclear dioxomolybdenum(vi) complexes 1-4 of general formula [(MoO2L)2(N-N)] with an ONS donor Schiff base ligand (H2L = S-benzyl-β-N-(5-bromo-2-hydroxyphenyl)methylenedithiocarbazate) and bridging auxiliary ligands having different leng

Ruthenium(II)–Arene Metallacycles: Crystal Structures, Interaction with DNA, and Cytotoxicity

A series of 24, 26-membered RuII2 metallamacrocycles containing 1-{3-[(1H-imidazol-1-yl)methyl]benzyl}-1H-imidazole (m-bib) and 1-{4-[(1H-imidazol-1-yl)methyl]benzyl}-1H-imidazole (p-bib) ligands have been synthesized and characteriz

An infinite 2D polyrotaxane network in Ag2(bix)3(NO3)2 (bix = 1,4-bis(imidazol-1-ylmethyl)benzene)

-

Bis-cationic ionic liquid crystals

A series of bis-cationic imidazolium-based compounds are reported, where two imidazolium head groups are bridged by different types of spacers: a saturated C6 hydrocarbon spacer (type A), an ether bridge (type B), a benzylic spacer (type C) and

IMIDAZOLIUM-QUATERNARY AMMONIUM COPOLYMERS AS NOVEL ANTIBACTERIAL AND ANTIFUNGAL MATERIALS

The present invention relates to quaternary ammonium-imidazolium copolymers having the following Formula (I): where the various groups are as defined in the specification. The present invention also relates to the polymer having the following Formula (II)