51833-36-4

Basic information

• Product Name: chloro(p-chlorophenyl)magnesium
• Synonyms: chloro(p-chlorophenyl)magnesium;4-Chlorophenylmagnesium chloride;p-chlorophenylmagnesiumchloride;(4-Chlorophenyl)chloromagnesium;Einecs 257-462-3;4-Chlorophenylmagnesium chloride 1M solution in THF;4-Chlorophenylmagnesium chloride 1M solution in DEE
• CAS NO: 51833-36-4
• Molecular Formula: C₆H₄Cl₂Mg
• Molecular Weight: 171.30696
• EINECS: 257-462-3
• Mol File: 51833-36-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 131.7°C at 760 mmHg
• Flash Point: 23.9°C
• Appearance: /
• Vapor Pressure: 11.2mmHg at 25°C
• CAS DataBase Reference: chloro(p-chlorophenyl)magnesium(CAS DataBase Reference)
• NIST Chemistry Reference: chloro(p-chlorophenyl)magnesium(51833-36-4)
• EPA Substance Registry System: chloro(p-chlorophenyl)magnesium(51833-36-4)

Safety Data

• Hazardous Substances Data: 51833-36-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C6H4Cl.ClH.Mg/c7-6-4-2-1-3-5-6;;/h2-5H;1H;/q-1;;+2/p-1

Upstream product

• 106-46-7 para-dichlorobenzene 
• 60-29-7 diethyl ether 
• 7553-56-2 iodine 
• 497-19-8 sodium carbonate 
• 106-39-8 bromochlorobenzene 

Downstream Products

• 3391-10-4 1-(p-chlorophenyl)ethyl alcohol 
• 83176-32-3 2,2-Bis-(4-chloro-phenyl)-N-(2-diethylamino-ethyl)-2-hydroxy-N-methyl-acetamide 
• 85-56-3 2-(4-chlorobenzoyl)benzoic acid 
• 28799-40-8 5,5-bis(4-chlorophenyl)dihydrofuran-2(3H)-one 
• 3984-34-7 4-(4-chlorophenyl)-4-oxobutanoic acid 
• 233765-22-5 methyl 2-methyl-2-<1-(3-benzoyl-4-para-chlorophenyl-1,4-dihydropyridyl)>acetate 
• 106364-41-4 p-(3-methyl-2-butenyl)phenyl magnesium chloride 
• 82593-99-5 tris-(p-chlorophenyl)butyltin 
• 66259-06-1 (4-chlorophenyl)dimethyl(vinyl)silane 
• 1242079-86-2 C₁₈H₁₄ClNO 
• 874498-25-6 4,7-dichloro-2-(4-chlorophenyl)quinoline 
• 25115-73-5 2-(4-chlorophenyl)cyclohexanone 
• 189810-98-8 1-(4-chlorophenyl)cyclopentane-1-carbaldehyde 
• 91767-46-3 1-(4-chlorophenyl)cyclohexane-1,2-diol 

Relevant articles and documents

Method of preparing organomagnesium compounds

The present invention is directed to a reagent for use in the preparation of organomagnesium compounds as well as to a method of preparing such organomagnesium compounds. The present invention furthermore provides a method of preparing functionalized or unfunctionalized organic compounds as well as the use of the reagents of the present invention in the preparation of organometallic compounds and their reaction with electrophiles. Finally, the present invention is directed to the use of lithium salts - LiY in the preparation of organometallic compounds and their reactions with electrophiles and to an organometallic compound which is obtainable by the disclosed method.

Tetraarylboron-ammonium complexes and their uses

New tetraarylboron-ammonium complexes having the general formula: STR1 wherein R1 represents a hydrogen or a halogen atom or a lower alkyl group; R2 represents a halogen atom or a lower alkyl or a lower alkenyl group; and R3/su