211292-60-3

Basic information

• Product Name: N-(2-methoxyphenyl)-2,5-dimethylaniline
• Synonyms: N-(2-methoxyphenyl)-2,5-dimethylaniline
• CAS NO: 211292-60-3
• Molecular Formula: C15H17NO
• Molecular Weight: 227.30158
• Mol File: 211292-60-3.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(2-methoxyphenyl)-2,5-dimethylaniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-methoxyphenyl)-2,5-dimethylaniline(211292-60-3)
• EPA Substance Registry System: N-(2-methoxyphenyl)-2,5-dimethylaniline(211292-60-3)

Safety Data

• Hazardous Substances Data: 211292-60-3(Hazardous Substances Data)

Usage

General Description

N-(2-methoxyphenyl)-2,5-dimethylaniline, also known as 2,5-dimethoxy-N-(2-methoxyphenyl)aniline, is an organic compound with the formula C15H17NO2. It is commonly used as an intermediate in the production of various dyes and pigments, as well as in the synthesis of pharmaceuticals and other organic compounds. This chemical is a white to light yellow solid with a melting point around 87-90°C and is sparingly soluble in water. It is important to handle this compound with care, as it may be harmful if ingested or inhaled, and can cause irritation to the skin and eyes.

Upstream product

• 95-72-7 2-chloro-1,4-dimethyl-benzene 
• 90-04-0 2-methoxy-phenylamine 
• 74-88-4 methyl iodide 
• 95-78-3 2,5-Dimethylaniline 
• 73939-13-6 N-(diphenylmethylene)-N-(2-methoxyphenyl)amine 
• 578-57-4 2-bromoanisole 
• 766-51-8 2-Chloroanisole 
• 553-94-6 4-bromo-m-xylene 

Relevant articles and documents

Preparation method of secondary aromatic amine

The invention provides a method for preparing secondary aromatic amine by performing a palladium-catalyzed C-N coupling reaction on (pseudo)aryl halide and (pseudo)heterocyclic aryl halide and primary(heterocyclic)aromatic amine. The method is characterized in that an alkali for promoting the reaction is an alkali metal carboxylate or an alkali metal bicarbonate.

Palladium-Catalyzed Synthesis of Diarylamines and 1- and 2-Oxygenated Carbazoles: Total Syntheses of Natural Alkaloids Clauraila A, Clausenal, Clausine P, and 7-Methoxy- O -methylmukonal

The scope and limitations of the strategy for the conversion of 2-anilinocyclohexenones and N -arylcyclohexane enaminones into the 1- and 2-oxygenated carbazole scaffolds, respectively, were evaluated. The one-pot palladium(0)-catalyzed aromatization/meth

(N-heterocyclic carbene)PdCl2(TEA) complexes: Studies on the effect of the "throw-away" ligand in catalytic activity

The synthesis and characterization of a series of (N-heterocyclic carbene)PdCl2(TEA) (TEA = triethylamine) complexes are presented. A comparison of their activity in the Suzuki-Miyaura and Buchwald-Hartwig reactions with similar (N-heterocyclic carbene)Pd(II) complexes is also presented.