5140-95-4

Usage

Structure

Substituted benzene

Explanation

The compound is a benzene ring with two substituents attached to it, making it a substituted benzene.

Explanation

The two substituents attached to the benzene ring are a bromomethyl group (-CH2Br) and a phenylethynyl group (-C≡C-C6H5), which contribute to the compound's reactivity and properties.

Explanation

The compound contains an alkyl halide functional group (bromomethyl) and an alkynyl functional group (phenylethynyl), which are responsible for its chemical reactivity.

Explanation

Due to its versatile chemical structure and reactivity, 1-(bromomethyl)-4-(phenylethynyl)benzene is used as a starting material in organic synthesis to create more complex molecules. It is also utilized in the production of pharmaceuticals and agrochemicals.

Explanation

The compound can be used as a building block in the development of new materials and compounds for various industrial applications, thanks to its unique structure and reactivity.

Explanation

Although the exact physical state is not provided, most organic compounds with a molecular weight similar to 1-(bromomethyl)-4-(phenylethynyl)benzene are solids or liquids at room temperature.

Explanation

The presence of the bromomethyl and phenylethynyl groups makes the compound reactive towards various types of reagents, such as nucleophiles, electrophiles, and organometallic compounds, allowing for further functionalization and synthesis of new molecules.

Substituents

Bromomethyl group and phenylethynyl group

Functional groups

Alkyl halide and alkynyl

Applications

Organic synthesis, pharmaceuticals, and agrochemicals

Industrial applications

Building block for new materials and compounds

Physical state

Likely a solid or liquid at room temperature

Reactivity

Reactive towards nucleophiles, electrophiles, and organometallic reagents

Upstream product

• 3287-02-3 4-(phenylethynyl)toluene 
• 536-74-3 phenylacetylene 
• 54737-75-6 (4-(phenylethynyl)phenyl)methanol 
• 18282-51-4 4-iodo-benzyl alcohol 
• 619-58-9 4-iodobenzoic acid 

Downstream Products

• 1278551-01-1 Br^(1-)*C₃₃H₂₅N₂⁽¹⁺⁾ 
• 1278551-00-0 1-methyl-3-((4-phenylethynyl)benzyl)imidazolium bromide 
• 1421636-51-2 1,3-bis(4-(phenylethynyl)benzyl)-1H-benzo[d]imidazol-3-iumbromide 
• 1421636-67-0 (4-phenylethynyl)benzyl benzimidazole 
• 1421636-53-4 (N,N’-diphenylethynylbenzyl)imidazolium tetrafluoroborate 
• 1421636-56-7 (N,N'-diphenylethynylbenzyl)imidazolium hexafluorophosphate 
• 1421636-60-3 (N,N'-diphenylethynylbenzyl)imidazolium bis(trifluoromethane)sulfonimide 
• 1445435-63-1 C₂₅H₂₄N₂O₂ 

Relevant academic research and scientific papers

Alkyne-functionalized superstable graphitic silver nanoparticles for raman imaging

Noble metals, especially gold, have been widely used in plasmon resonance applications. Although silver has a larger optical cross section and lower cost than gold, it has attracted much less attention because of its easy corrosion, thereby degrading plas

Benzimidazolium salts prevent and disrupt methicillin-resistant: Staphylococcus aureus biofilms

Emergence of resistant bacteria encourages us to develop new antibiotics and strategies to compensate for the different mechanisms of resistance they acquire. One of the defense mechanisms of resistant bacteria is the formation of biofilms. Herein we show

Palladium-catalyzed silylation reaction between benzylic halides and silylboronate

An efficient Pd-catalyzed silylation reaction of benzylic halides with silylboronate is reported. In this reaction, primary and secondary benzylic halides could react well with silylboronates to afford benzylic silanes. This reaction accommodates a broad substrate scope and proceeds smoothly under very mild reaction conditions. The corresponding products could be obtained in moderate to high yields and with stereospecificity.

Support-free palladium-NHC catalyst for highly recyclable heterogeneous suzuki-miyaura coupling in neat water

Among the various new challenges of chemical processes in water, research on stable, highly active, and recyclable catalysts is a prosperous field. We present here a palladium-NHC catalyst that was synthesized with good yields through a series of simple synthetic steps. This organometallic species was used as a heterogeneous catalyst in low loadings for Suzuki-Miyaura coupling in neat water, under mild conditions. Reaction conditions were optimized for a simple, green, and support-free procedure, without using any phase transfer agent. The catalyst shows excellent reactivity in short times toward different substrates and a very good recyclability.

Benzimidazolium-based synthetic chloride and calcium transporters in bacterial membranes

Herein, we present the first example of a benzimidazolium-based artificial transmembrane chloride transporter and a synthetic calcium ionophore that can regulate intracellular calcium concentrations in bacteria.

Uncovering new properties of imidazolium salts: Cl- transport and supramolecular regulation of their transmembrane activity

We report the Cl- transport activity for three imidazolium-based transporters. We present significant findings regarding the use of α-cyclodextrin and cucurbit[7]uril macrocycles to form inclusion complexes with these salts and to inhibit their

MULTICYCLIC TERTIARY AMINE POLYAROMATIC SQUALENE SYNTHASE INHIBITORS

This invention relates to polycyclic compounds containing two mono- and/or bicyclic rings and a basic tertiary amino group capable of forming an ammonium ion at biological pH and which reduces levels of serum cholesterol in the body without significantly reducing mevalonic metabolite synthesis. This invention relates also to pharmacological compositions and method of treatment for lowering serum cholesterol levels using the compounds of this invention. The compounds of this invention are described by the formula where Ar I is phenylene or naphthylene, Ar II is phenyl or naphthyl and A is 1-azabicyclo[2.2.2]octan-3-yl