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

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 a white to light yellow solid with a melting point around 87-90°C and is sparingly soluble in water. N-(2-methoxyphenyl)-2,5-dimethylaniline 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.

Uses

Used in Dye and Pigment Production:
N-(2-methoxyphenyl)-2,5-dimethylaniline is used as an intermediate in the production of various dyes and pigments. Its unique chemical structure allows for the creation of a wide range of colors and properties in these products.
Used in Pharmaceutical Synthesis:
N-(2-methoxyphenyl)-2,5-dimethylaniline is also used as an intermediate in the synthesis of pharmaceuticals. Its presence in the production process can contribute to the development of new medications and therapies.
Used in Organic Compound Synthesis:
N-(2-methoxyphenyl)-2,5-dimethylaniline is utilized in the synthesis of other organic compounds, demonstrating its versatility in various chemical reactions and applications.
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

• 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 
• 95-72-7 2-chloro-1,4-dimethyl-benzene 
• 90-04-0 2-methoxy-phenylamine 
• 553-94-6 4-bromo-m-xylene 

Relevant articles and documents

A terphenyl phosphine as a highly efficient ligand for palladium-catalysed amination of aryl halides with 1° anilines

A terphenyl phosphine ligand (2,6-bis(2,4,6-triisopropylphenyl)phenyl-dicyclohexylphosphine, TXPhos) and its supported palladium complex [(TXPhos)(allyl)PdCl] have been developed and the catalyst system is highly efficient in amination of aryl halides with 1° anilines, especially effective for densely functionalized substrates including both partners possessing ortho-ester, acetyl, nitrile and nitro groups. With the TXPhos-supported catalyst system, many partner combinations have been unprecedentedly realized and the base scope has been even extended to KOAc, which is even the best choice in the amination of 2-nitrochlorobenzene.

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.