571903-64-5

Basic information

• Product Name: Magnesium, chloro[4-(ethoxycarbonyl)phenyl]-
• CAS NO: 571903-64-5
• Molecular Formula: C9H9ClMgO2
• Molecular Weight: 208.927
• Mol File: 571903-64-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Magnesium, chloro[4-(ethoxycarbonyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Magnesium, chloro[4-(ethoxycarbonyl)phenyl]-(571903-64-5)
• EPA Substance Registry System: Magnesium, chloro[4-(ethoxycarbonyl)phenyl]-(571903-64-5)

Safety Data

• Hazardous Substances Data: 571903-64-5(Hazardous Substances Data)

Upstream product

• 5798-75-4 Ethyl 4-bromobenzoate 
• 51934-41-9 4-iodobenzoic acid ethyl ester 

Downstream Products

• 64678-66-6 ethyl 4-(phenylamino)benzoate 
• 50670-76-3 ethyl 4-hydroxy-4-biphenyl carboxylate 
• 70917-02-1 ethyl 4′-formyl[1,1′-biphenyl]-4-carboxylate 
• 720-44-5 1-(4-methoxyphenyl)-1-phenylmethanol 
• 85609-05-8 ethyl p-(hydroxy(phenyl)methyl)benzoate 
• 1379793-77-7 ethyl 4-(1-(3,4,5-trimethoxyphenyl)vinyl)benzoate 
• 959141-01-6 4-cyclohexyl-benzoic acid ethyl ester 
• 1173372-16-1 ethyl 4-(3-(furan-2-yl)propyl)benzoate 
• 86911-10-6 ethyl 4-(3-chloropropyl)benzoate 
• 2132-80-1 4,4'-Dimethoxybiphenyl 
• 732-80-9 4'-methoxy-biphenyl-4-carboxylic acid ethyl ester 
• 47230-38-6 diethyl biphenyl-4,4'-dicarboxylate 

Relevant articles and documents

Sequential nucleophilic addition/1,2-rearrangement of N-iminolactam: A ring-contractive strategy for the synthesis of 2-acyl pyrrolidines

A sequential nucleophilic addition/ring contraction of α-bromo N-iminolactam with organometallic reagents for the synthesis of 2-acyl pyrrolidines has been developed. The reaction allows facial construction of 2-acyl pyrrolidines incorporating not only ar

Cobalt-catalyzed addition of arylzinc reagents to alkynes to form ortho-alkenylarylzinc species through 1,4-cobalt migration

Migratory carbometalation: A cobalt-Xantphos complex catalyzes the addition of an arylzinc reagent to an unactivated internal alkyne; the reaction most likely involves insertion of the alkyne into an arylcobalt species and vinyl-to-aryl 1,4-cobalt migration, followed by transmetalation with the arylzinc reagent. Interception of the resulting ortho-alkenylarylzinc species with electrophiles allows access to 1-alkenyl arenes functionalized in the 2-position. Copyright

Iron-catalyzed aryl-aryl cross-couplings with magnesium-derived copper reagents

(Chemical Equation Presented) Well-matched couples: Functionalized aryl and heteroaryl copper species obtained from the corresponding magnesium derivatives undergo Fe-catalyzed cross-coupling reactions with aryl iodides that bear keto, ester, triflate, or nitrile groups (see scheme).