2362-36-9

Basic information

• Product Name: Benzene, 1-(1-chloroethyl)-4-methyl-
• CAS NO: 2362-36-9
• Molecular Formula: C9H11Cl
• Molecular Weight: 154.639
• Mol File: 2362-36-9.mol
• Article Data: 20

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(1-chloroethyl)-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(1-chloroethyl)-4-methyl-(2362-36-9)
• EPA Substance Registry System: Benzene, 1-(1-chloroethyl)-4-methyl-(2362-36-9)

Safety Data

• Hazardous Substances Data: 2362-36-9(Hazardous Substances Data)

Upstream product

• 123-91-1 1,4-dioxane 
• 140863-24-7 1-(P-tolyl)ethyl chloroformate 
• 536-50-5 CH₃C₆H₄CH(CH₃)OH 
• 42070-98-4 1-(p-tolyl)ethylamine 
• 122-00-9 para-methylacetophenone 
• 91563-27-8 N-(1-p-tolylethyl)propionamide 
• 108-88-3 toluene 
• 622-97-9 1-ethenyl-4-methylbenzene 

Downstream Products

• 536-50-5 CH₃C₆H₄CH(CH₃)OH 
• 111662-73-8 1-(4-methylphenyl)ethyl ethyl ether 
• 86561-30-0 1-(4-methylphenyl)ethyl acetate 
• 91633-31-7 1-(para-methylphenyl)-1-azidoethane 
• 66398-70-7 1-methyl-4-(1-prop-2-ynyloxy-ethyl)-benzene 
• 79744-75-5 4-methyl-1-methoxyethylbenzene 
• 622-97-9 1-ethenyl-4-methylbenzene 
• 88093-49-6 2-tert.-butyl-4-chloro-5-(4,α-dimethylbenzyloxy)-3-(2H)-pyridazinone 
• 60263-86-7 2-(1-[4-methylphenyl]ethylsulfonyl) pyridine N-oxide 
• 1220528-68-6 C₁₄H₂₀ 
• 1220528-67-5 1-(1-methylcyclopropyl)-2-(4-methylphenyl)propane 
• 1554032-18-6 1-phenyl-2-{1-(4-tolyl)ethyl}-propen-1-one 

Relevant articles and documents

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Iron-catalysed enantioconvergent Suzuki-Miyaura cross-coupling to afford enantioenriched 1,1-diarylalkanes

The first stereoconvergent Suzuki-Miyaura cross-coupling reaction was developed to afford enantioenriched 1,1-diarylalkanes. An iron-based complex containing a chiral cyanobis(oxazoline) ligand framework was best to obtain enantioenriched 1,1-diarylalkanes from cross-coupling reactions between unactivated aryl boronic esters and benzylic chlorides. Enhanced yields were obtained when 1,3,5-trimethoxybenzene was used as an additive, which is hypothesized to extend the lifetime of the iron-based catalyst. Exceptional enantioselectivities were obtained with challenging ortho-substituted benzylic chlorides. This journal is

Novel synthesizing method of 2-(4-bromomethyl)phenylpropionic acid

The invention belongs to the field of preparation of intermediates in chemical engineering, and particularly relates to a novel synthesizing method of 2-(4-bromomethyl)phenylpropionic acid. The novelsynthesizing method comprises the following steps of using 4-methyl acetophenone as the raw material; performing reduction, chlorinating and cyaniding, so as to obtain 2-(4-methyl)phenylpropionitrile;hydrolyzing, and brominating, so as to obtain the 2-(4-bromomethyl)phenylpropionic acid. The novel synthesizing method has the advantages that the yield rate is increased, and the cost of raw material is low; the novel synthesizing method is suitable for industrialized production.