7510-28-3

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
1-(Chloromethyl)-2-(phenylmethyl)benzene is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals for its ability to facilitate the creation of complex organic molecules that are integral to the development of new drugs and pesticides.
Used in Specialty Polymers and Resins Production:
In the polymer and resin industry, 1-(Chloromethyl)-2-(phenylmethyl)benzene is used as a key component in the production of specialty polymers and resins, contributing to the development of materials with unique properties for specific applications.
Used in Organic Synthesis:
As a versatile building block, 1-(Chloromethyl)-2-(phenylmethyl)benzene is used in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds, which are crucial in constructing a wide range of organic compounds.
Used in the Preparation of Arylated Compounds:
1-(Chloromethyl)-2-(phenylmethyl)benzene is utilized as a reagent in the preparation of arylated compounds, which are important in various chemical reactions and have applications in different fields of chemistry.
Used in Chemical Reactions such as Alcohol to Alkyl Chloride Conversion:
1-(Chloromethyl)-2-(phenylmethyl)benzene serves as a useful reagent in chemical reactions, including the conversion of alcohols to alkyl chlorides, a transformation that is significant in the synthesis of various organic compounds.
Safety Note:
It is important to handle 1-(Chloromethyl)-2-(phenylmethyl)benzene with caution due to its potential mutagenic and carcinogenic properties. Proper safety measures should be implemented to minimize health risks during its use in chemical processes.

InChI:InChI=1/C14H13Cl/c15-11-14-9-5-4-8-13(14)10-12-6-2-1-3-7-12/h1-9H,10-11H2

Upstream product

• 1586-00-1 2-(benzyl)benzyl alcohol 
• 100-44-7 benzyl chloride 
• 7446-70-0 aluminium trichloride 
• 98-95-3 nitrobenzene 
• 71-43-2 benzene 
• 85-52-9 2-Benzoylbenzoic acid 
• 612-35-1 2-Benzylbenzoic acid 

Downstream Products

• 36374-49-9 2-(2-benzylphenyl)acetic acid 
• 6196-39-0 1-(2-benzylphenyl)-N,N-dimethylmethanamine 
• 120-12-7 anthracene 

Relevant academic research and scientific papers

Method for preparing coupling arene from aryl halide by ionizing, discharging and coupling

The invention discloses a method for preparing coupling arene from aryl halide by ionizing, discharging and coupling. The method comprises the following steps: placing a magnetic stirrer into a three-necked flask and adding aryl halide occupying 1/2 flask, thereby finishing the assembling of an ionizing reaction device; placing the ionizing reaction device into an oil bath pan, introducing inert gas into a reaction system, removing air from the reaction system, starting stirring and heating in the oil bath pan to make aryl halide flow back, and meanwhile, introducing water into a ball-shaped condensation pipe for cooling; starting a high-voltage power generator, and introducing powerful arc generated into the three-necked flask through a metal electrode, thereby ionizing and decomposing aryl halide steam and generating a coupling arene compound; stopping ionizing and heating when solids are separated or the backflow of aryl halide is slowed in a round-bottom flask, and then ending the reaction; recrystallizing or performing reduced pressure distillation purification on the coupling arene product in the flask, thereby acquiring the coupling arene product. The method disclosed by the invention has the advantages of low cost, high efficiency, environmental protection, and the like.

MODULATORS OF C3A RECEPTOR AND METHODS OF USE THEREOF

Provided are compounds that are modulators of C3a receptor activity, compositions containing the compounds and methods of use of the compounds and compositions. In certain embodiments, the compounds are pyridones. In certain embodiments, provided are methods for treatment or amelioration of diseases associated with modulation of C3a receptor activity.

Probing the active catalytic sites of zeolites with benzyl chloride

Zeolites contain numerous catalytic sites. In order to conduct organic chemistry properly, it is necessary to know which site catalyzes the reaction. The conversion of benzyl chloride was tested as a probe reaction. Different products are obtained when th

Lithium tetrakis(pentafluorophenyl)borate-catalyzed Friedel-Crafts benzylation reactions

Lithium tetrakis(pentafluorophenyl)borate [LiB(C6F5)4], a neutral salt, effectively catalyzed Friedel-Crafts benzylation reactions of aromatic compounds with benzyl chloride or mesylate and their substituted derivatives. The LiB(C6F5)4-catalyzed reactions proceeded more efficiently in the coexistence of magnesium oxide.