92115-23-6

Basic information

• Product Name: Benzenamine, N-ethyl-4-methoxy-N-phenyl-
• CAS NO: 92115-23-6
• Molecular Formula: C15H17NO
• Molecular Weight: 227.306
• Mol File: 92115-23-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-ethyl-4-methoxy-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-ethyl-4-methoxy-N-phenyl-(92115-23-6)
• EPA Substance Registry System: Benzenamine, N-ethyl-4-methoxy-N-phenyl-(92115-23-6)

Safety Data

• Hazardous Substances Data: 92115-23-6(Hazardous Substances Data)

Upstream product

• 104-48-3 4-methoxy-N-ethylaniline 
• 637-88-7 1,4-Cyclohexanedione 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 103-69-5 N-ethyl-N-phenylamine 
• 101089-92-3 O-benzoyl-N-ethyl-N-phenylhydroxylamine 
• 7447-59-8 N-ethyl-N-phenylhydroxylamine 
• 100-65-2 N-Phenylhydroxylamine 

Relevant articles and documents

Cobalt-Catalyzed Electrophilic Amination of Aryl- and Heteroarylzinc Pivalates with N-Hydroxylamine Benzoates

Aryl- and heteroarylzinc pivalates can be aminated with O-benzoylhydroxylamines at 25 °C within 2–4 h in the presence of 2.5–5.0 % CoCl2?2 LiCl to furnish the corresponding tertiary arylated or heteroarylated amines in good yields. This electrophilic amination also provides access to diarylamines and aryl(heteroaryl)amines. A new tuberculosis drug candidate (Q203) was prepared in six steps and 56 % overall yield by using this cobalt-catalyzed amination as the key step.

Palladium-Catalyzed Amination of Aryl Bromides: Use of Phosphinoether Ligands for the Efficient Coupling of Acyclic Secondary Amines

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