64053-59-4

Basic information

• Product Name: Acetamide, 2-chloro-N-(3-methoxyphenyl)-N-phenyl-
• CAS NO: 64053-59-4
• Molecular Formula: C15H14ClNO2
• Molecular Weight: 275.735
• Mol File: 64053-59-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Acetamide, 2-chloro-N-(3-methoxyphenyl)-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, 2-chloro-N-(3-methoxyphenyl)-N-phenyl-(64053-59-4)
• EPA Substance Registry System: Acetamide, 2-chloro-N-(3-methoxyphenyl)-N-phenyl-(64053-59-4)

Safety Data

• Hazardous Substances Data: 64053-59-4(Hazardous Substances Data)

Upstream product

• 536-90-3 m-Anisidine 
• 591-50-4 iodobenzene 
• 101-16-6 3-methoxy-N-phenylaniline 
• 79-04-9 chloroacetyl chloride 

Downstream Products

• 83254-82-4 6-methoxy-1-phenyl-1,3-dihydro-indol-2-one 
• 83254-80-2 4-Methoxy-1-phenyl-1,3-dihydro-indol-2-one 
• 344307-16-0 4-Hydroxy-1-phenyl-1,3-dihydro-indol-2-one 
• 64053-58-3 6-Hydroxy-1-phenyl-1,3-dihydro-indol-2-one 

Relevant articles and documents

MONO(m-SUBSTITUTED) CHLOROACETYLDIARYLAMINES IN THE STOLLE REACTION

The effect of substituted (OCH3, Cl) on the ratio of the isomeric N-aryloxindoles formed in the Stolle reaction from mono(m-substituted) chloroacetyldiarylamines was studied.It was shown by means of gas-liquid chromatography (GLC) and PMR spectroscopy that in the case of the methoxy group electrophilic substitution occurs only in the ring activated by the substituent.The presence of a halogen atom leads only to 1-(m-chlorophenyl)oxindole.The results show that high selectivity of the attack by the carbonium ion on the phenyl rings with electron-donor and electron-acceptor substituents is also retained in the case of intramolecular electrophilic substitution under conditions of kinetic control.