75681-30-0

Basic information

• Product Name: 1-(4-methoxyphenyl)-2-(methyl(phenyl)amino)ethan-1-one
• Synonyms: 1-(4-methoxyphenyl)-2-(methyl(phenyl)amino)ethan-1-one
• CAS NO: 75681-30-0
• Molecular Weight: 255.316
• Mol File: 75681-30-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(4-methoxyphenyl)-2-(methyl(phenyl)amino)ethan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-methoxyphenyl)-2-(methyl(phenyl)amino)ethan-1-one(75681-30-0)
• EPA Substance Registry System: 1-(4-methoxyphenyl)-2-(methyl(phenyl)amino)ethan-1-one(75681-30-0)

Safety Data

• Hazardous Substances Data: 75681-30-0(Hazardous Substances Data)

Upstream product

• 75681-34-4 N/methyl-N-phenylaminomethyl 2-naphthyl ketone 
• 75681-35-5 2-(N-methylanilino)indan-1-one 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 172984-02-0 N-(2-iodoanilinomethyl)succinimide 
• 57056-93-6 N-methyl-2-iodoaniline 
• 172983-94-7 2-[(2-Iodo-phenyl)-methyl-amino]-1-(4-methoxy-phenyl)-ethanone 
• 100-61-8 N-methylaniline 
• 79409-10-2 2-(Diphenyl-phosphinoyl)-1-(4-methoxy-phenyl)-2-(methyl-phenyl-amino)-ethanol 

Downstream Products

• 62082-46-6 3-(p-methoxyphenyl)-1-phenylazetidin-3-ol 
• 2513-64-6 1,3-diphenylimidazolidine 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 1017609-37-8 YWI₉₂ 
• 86896-39-1 2-(4-methoxyphenyl)-N-methyl-2-oxo-N-phenylacetamide 
• 1476035-08-1 1-(4-methoxyphenyl)-2-(2-phenyl-1H-indol-3-yl)ethane-1,2-dione 
• 130289-80-4 1-(1H-indol-3-yl)-2-(4-methoxyphenyl)ethane-1,2-dione 
• 51206-77-0 3-(4-methoxyphenyl)-1-methyl-1H-indole 
• 100-09-4 4-methoxybenzoic acid 
• 93-61-8 N-methyl-N-phenylformamide 

Relevant articles and documents

Construction of indole skeletons by sequential actions of sunlight and rhodium on α-aminoacetophenones

Indole skeletons were constructed from 2-(N-aryl-N-methylamino) acetophenones by the sequential actions of sunlight and a rhodium catalyst. This method presents an example of the direct use of sunlight in organic synthesis.

NOVEL APPLICATIONS OF α-AMINOSUBSTITUTED DIPHENYLPHOSPHINE OXIDES. THE CONVERSION OF ALDEHYDES INTO α-AMINOMETHYLKETONES.

Aromatic and aliphatic aldehydes (R3CHO) can be converted into α-aminomethylketones (R3COCH2NR1R2) via reaction with (α-aminomethyl)diphenylphosphine oxides.