3062-48-4

Basic information

• Product Name: 2-(2-ETHOXYETHOXY)ANILINE
• Synonyms: AKOS BC-2514;2-(2-ETHOXYETHOXY)ANILINE;CHEMBRDG-BB 4024089;UKRORGSYN-BB BBV-108402;2-(2-ethoxyethoxy)aniline(SALTDATA: HCl)
• CAS NO: 3062-48-4
• Molecular Formula: C₁₀H₁₅NO₂
• Molecular Weight: 181.2316
• Mol File: 3062-48-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 296.933°C at 760 mmHg
• Flash Point: 145.264°C
• Appearance: /
• Density: 1.056g/cm³
• Vapor Pressure: 0.001mmHg at 25°C
• Refractive Index: 1.528
• PKA: 4.31±0.10(Predicted)
• CAS DataBase Reference: 2-(2-ETHOXYETHOXY)ANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-ETHOXYETHOXY)ANILINE(3062-48-4)
• EPA Substance Registry System: 2-(2-ETHOXYETHOXY)ANILINE(3062-48-4)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 3062-48-4(Hazardous Substances Data)

Usage

Appearance

Pale yellow to dark brown liquid

Odor

Faint aromatic

Usage

Intermediate in the production of dyes, pharmaceuticals, and other organic compounds; chemical building block in the synthesis of various polymers and resins

Toxicity

Not highly toxic, but exposure to high concentrations may cause irritation to the skin, eyes, and respiratory system

Safety

Handle with care and follow proper safety protocols

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

Upstream product

• 176324-78-0 1-[2-(2-Iodo-ethoxy)-ethoxy]-2-nitro-benzene 
• 88-75-5 2-hydroxynitrobenzene 
• 3062-47-3 2-nitrophenyl (2-ethoxyethyl) ether 

Relevant articles and documents

Synthesis of new dibenzo-diaza-crown ethers

A new method for the synthesis of dibenzo-diaza-crown ethers involving the 1:1-cyclocondensation of α,ω-contrafunctional amines is reported.

Process for making N-(N'-methylenepyrrolidonyl)-2-substituted anilines

This invention relates to a process for making N-(N'-methylenepyrrolidonyl)-2-substituted anilines in high yield. The products are useful intermediates in the synthesis of herbicides. The process comprises reacting substantially equivalent molar concentrations of a 2-substituted aniline, as defined herein, with N-methylolpyrrolidone in an aromatic hydrocarbon solvent in the absence of an acid or base catalyst at a reflux temperature of 80°-140° C. while simultaneously and continuously distilling out from the reaction mixture an azeotrope consisting essentially of water and solvent until substantially all the water produced during the reaction has been removed thereby, and, thereafter, crystallizing the product from the remaining solution.

Herbicidal n-(haloacetyl)-n-(n-methylene pyrrolidonyl)-2-oxyalkyleneoxyalkylanilines

Herbicidal compounds having the formula: STR1 where n is 1-3, R is alkyl of 1-3 carbon atoms, R' is hydrogen or alkyl of 1-3 carbon atoms, and x is chloro or bromo, are disclosed herein. The compounds of the invention show good herbicidal activity, especi