26972-56-5

Usage

Uses

Used in Chemical Synthesis:
N-(2,2-dimethoxyethyl)aniline is used as an intermediate in the production of various products, such as dyes, pharmaceuticals, and agrochemicals. Its unique structure allows it to be a versatile building block in the synthesis of a wide range of compounds.
Used in Corrosion Inhibition:
N-(2,2-dimethoxyethyl)aniline serves as a corrosion inhibitor, protecting materials from the damaging effects of corrosion. Its application helps to extend the lifespan and maintain the integrity of various industrial equipment and structures.
Used in Organic Synthesis as a Reagent:
N-(2,2-dimethoxyethyl)aniline is utilized as a reagent in organic synthesis, facilitating various chemical reactions and processes. Its presence can enhance the efficiency and selectivity of reactions, contributing to the production of desired products.

InChI:InChI=1/C10H15NO2/c1-12-10(13-2)8-11-9-6-4-3-5-7-9/h3-7,10-11H,8H2,1-2H3

Upstream product

• 62-53-3 aniline 
• 97-97-2 chloroacetaldehyde dimethyl acetal 

Downstream Products

• 60117-33-1 4-(hexafluoro-2-hydroxy-2-propyl)anilinoacetaldehyde dimethyl acetal 
• 288371-91-5 3-[(methoxy)methoxy]-1-phenyl-4-[2-(trimethylsilyl)ethynyl]-2-imidazolidinone 
• 288371-94-8 4-ethynyl-3-hydroxy-1-phenyl-2-imidazolidinone 
• 288371-85-7 (2-oxoethyl)phenylcarbamic acid methyl ester 
• 70040-54-9 {3-[(2,2-Dimethoxy-ethyl)-phenyl-carbamoyloxy]-phenyl}-carbamic acid 2-methoxy-ethyl ester 
• 70039-92-8 {3-[(2,2-Dimethoxy-ethyl)-phenyl-carbamoyloxy]-phenyl}-carbamic acid prop-2-ynyl ester 
• 70039-91-7 {3-[(2,2-Dimethoxy-ethyl)-phenyl-carbamoyloxy]-phenyl}-carbamic acid allyl ester 
• 70039-95-1 (2,2-Dimethoxy-ethyl)-phenyl-carbamic acid 3-ethylsulfanylcarbonylamino-phenyl ester 
• 70039-82-6 {3-[(2,2-Dimethoxy-ethyl)-phenyl-carbamoyloxy]-phenyl}-carbamic acid methyl ester 
• 70039-94-0 (2,2-Dimethoxy-ethyl)-phenyl-carbamic acid 3-methylsulfanylcarbonylamino-phenyl ester 
• 70039-85-9 {3-[(2,2-Dimethoxy-ethyl)-phenyl-carbamoyloxy]-phenyl}-carbamic acid isopropyl ester 
• 70040-52-7 {3-[(2,2-Dimethoxy-ethyl)-phenyl-carbamoyloxy]-phenyl}-carbamic acid 2-chloro-1-methyl-ethyl ester 
• 70040-53-8 {3-[(2,2-Dimethoxy-ethyl)-phenyl-carbamoyloxy]-phenyl}-carbamic acid 2-bromo-ethyl ester 
• 70040-19-6 {3-[(2,2-Dimethoxy-ethyl)-phenyl-carbamoyloxy]-phenyl}-carbamic acid sec-butyl ester 

Relevant academic research and scientific papers

Access to Unsymmetrically Substituted Diaryl Gold N-Acyclic Carbene (NAC) and N-Heterocyclic Carbene (NHC) Complexes via the Isonitrile Route

A variety of unsymmetric diaryl gold N-acyclic carbene (NAC) complexes was synthesized via the isonitrile route by three different methods: (a) solvent free in a melt, (b) mechanochemically and (c) in THF at room temperature. The latter method can also be used to synthesize unsaturated gold NHC complexes. These methods overall offer access to a broad array of new complexes and remove one of the previous limitations of the isonitrile route to NAC and NHC complexes of gold, namely the inability to react with the less nucleophilic aromatic amines. The new complexes also proved to be successful as pre-catalysts in the gold-catalyzed phenol synthesis. (Figure presented.).

Ultrasound assisted one-pot synthesis of benzo-fused indole-4,9-dinones from 1,4-naphthoquinone and α-aminoacetals

A one-pot synthesis of benzo[f]indole-4,9-diones from 1,4-naphthoquinone with α-aminoacetals has been developed. This method provides a straightforward synthesis of benzo[f]indole-4,9-diones via intramolecular nucleophilic attack of aminoquinones to aldehydes under mild reaction conditions. The detailed mechanism was also investigated.