2125-35-1

Basic information

• Product Name: ethyl 4-chloro-4-phenylbutanoate
• Synonyms: ethyl 4-chloro-4-phenylbutanoate
• CAS NO: 2125-35-1
• Molecular Weight: 226.703
• Mol File: 2125-35-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: ethyl 4-chloro-4-phenylbutanoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 4-chloro-4-phenylbutanoate(2125-35-1)
• EPA Substance Registry System: ethyl 4-chloro-4-phenylbutanoate(2125-35-1)

Safety Data

• Hazardous Substances Data: 2125-35-1(Hazardous Substances Data)

Upstream product

• 2051-95-8 succinylbenzene 
• 71-43-2 benzene 
• 100-42-5 styrene 
• 105-39-5 chloroacetic acid ethyl ester 
• 65-85-0 benzoic acid 
• 100-52-7 benzaldehyde 
• 911641-23-1 bis(2-carboethoxyethyl)zinc 
• 98-88-4 benzoyl chloride 
• 27374-25-0 [(1-Ethoxycyclopropyl)oxy]trimethylsilane 
• 1008-76-0 4,5-dihydro-5-phenyl-2(3H)-furanone 
• 64-17-5 ethanol 

Downstream Products

• 6270-17-3 ethyl 3-benzoylpropanoate 

Relevant articles and documents

Atom transfer radical addition (ATRA) of carbon tetrachloride and chlorinated esters to various olefins catalyzed by Cp′Ru(PPh 3)(PR3)Cl complexes

CpRu(PPh3)(PR3)Cl complexes, where PR 3 = PMe3, PPh3, or PTA (PTA = 1,3,5-triaza-7-phosphaadamantane), were used to catalyze the atom transfer radical addition of chlorinated esters (CClsu

Exploring the substrate scope of the Ru(II)-catalyzed kharasch reaction

The Kharasch reaction, or atom-transfer addition of polyhalogenated alkanes to alkenes is known to be catalyzed by a number of Ru(II) complexes. The easily prepared [RuCl2(PPh3)3] was used to investigate the reaction scope. A number of halogenated alkanes were added to a range of alkenes with good to excellent regioselectivities.