113138-08-2

Basic information

• Product Name: Ethanone, 1-[4-(3-phenylpropyl)phenyl]-
• CAS NO: 113138-08-2
• Molecular Formula: C17H18O
• Molecular Weight: 238.329
• Mol File: 113138-08-2.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[4-(3-phenylpropyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[4-(3-phenylpropyl)phenyl]-(113138-08-2)
• EPA Substance Registry System: Ethanone, 1-[4-(3-phenylpropyl)phenyl]-(113138-08-2)

Safety Data

• Hazardous Substances Data: 113138-08-2(Hazardous Substances Data)

Upstream product

• 637-59-2 1-Bromo-3-phenylpropane 
• 99-90-1 para-bromoacetophenone 
• 13329-40-3 4-Iodoacetophenone 
• 4119-41-9 1-iodo-3-phenylpropan 
• 104-52-9 phenylpropyl chloride 
• 99-91-2 para-chloroacetophenone 
• 329685-40-7 4,4,5,5-tetramethyl-2-(3-phenylpropyl)-[1,3,2]dioxaborolane 
• 1821-12-1 4-Phenylbutyric acid 
• 1081-75-0 1,3-diphenylpropane 
• 300-57-2 allylbenzene 
• 109613-00-5 4-acetophenyl triflate 
• 36329-85-8 (3-phenylpropyl)boronic acid 
• 108-24-7 acetic anhydride 

Downstream Products

• 857540-54-6 4-[3-(4-propionyl-phenyl)-propyl]-benzoic acid 
• 201138-62-7 4-{3-[4-(2-methoxycarbonyl-ethyl)-phenyl]-propyl}-benzoic acid methyl ester 
• 38320-54-6 (E)-3-[4-(3-Phenyl-propyl)-phenyl]-but-2-enoic acid methyl ester 
• 6337-66-2 4-(3-phenyl-propyl)-benzoic acid 

Relevant articles and documents

Nickel-catalysed cross-electrophile coupling of aryl bromides and primary alkyl bromides

The structure of primary alkylated arenes plays an important role in the molecular action of drugs and natural products. The nickel/spiro-bidentate-pyox catalysed cross-electrophile coupling of aryl bromides and primary alkyl bromides was developed for th

Preparation of Alkyl Indium Reagents by Iodine-Catalyzed Direct Indium Insertion and Their Applications in Cross-Coupling Reactions

An efficient method for the synthesis of alkyl indium reagent by means of an iodine-catalyzed direct indium insertion into alkyl iodide in THF is reported. The thus-generated alkyl indium reagents effectively underwent Pd-catalyzed cross-coupling reactions with various aryl halides, exhibiting good compatibility to a variety of sensitive functional groups. By replacing THF with DMA and using 0.75 equiv of iodine, less reactive alkyl bromide could be used as substrate for indium insertion with equal ease.

Copper(II)-catalyzed preparation of alkylindium compounds and applications in cross-coupling reactions both in aqueous media

An efficient water-based method for the synthesis of alkylindium compound in the presence of a catalytic amount of cheap and readily available CuSO4·5H2O (10 mol%) was developed. The thus-generated alkylindium compounds effectively underwent palladium-catalyzed cross-coupling reactions with a myriad of aryl halides in aqueous media, leading to the cross-coupled products in modest to high yields. The mildness of the formed alkyl organometallics allowed the tolerance to various important functional groups incorporated in both substrates of alkyl iodides and aryl halides.