26972-56-5

Basic information

• Product Name: N-(2,2-dimethoxyethyl)aniline
• Synonyms: N-(2,2-dimethoxyethyl)aniline;N-(2,2-Dimethoxyethyl)benzenamine
• CAS NO: 26972-56-5
• Molecular Formula: C₁₀H₁₅NO₂
• Molecular Weight: 181.2316
• EINECS: 248-149-2
• Mol File: 26972-56-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 288.5 °C at 760 mmHg
• Flash Point: 114.4 °C
• Appearance: /
• Density: 1.056 g/cm³
• Vapor Pressure: 0.00233mmHg at 25°C
• Refractive Index: 1.532
• CAS DataBase Reference: N-(2,2-dimethoxyethyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2,2-dimethoxyethyl)aniline(26972-56-5)
• EPA Substance Registry System: N-(2,2-dimethoxyethyl)aniline(26972-56-5)

Safety Data

• Hazardous Substances Data: 26972-56-5(Hazardous Substances Data)

Usage

Description

N-(2,2-dimethoxyethyl)aniline is an organic compound consisting of an aniline group (C6H5NH-) linked to a 2,2-dimethoxyethyl group (-OCH2CH2OCH3). It is characterized by its pale yellow to brown liquid appearance and a molecular formula of C10H15NO2.

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

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

Downstream Products

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

Relevant articles and documents

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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.