38954-40-4

Basic information

• Product Name: 2-(ethylphenylamino)ethyl acetate
• Synonyms: 2-(ethylphenylamino)ethyl acetate;N-(2-Acetoxyethyl)-N-ethylaniline;N-Ethyl-N-(2-acetoxyethyl)aniline;2-(N-ETHYLANILINO)-ETHYL ACETATE
• CAS NO: 38954-40-4
• Molecular Formula: C₁₂H₁₇NO₂
• Molecular Weight: 207.26888
• EINECS: 254-218-8
• Mol File: 38954-40-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 302.8 °C at 760 mmHg
• Flash Point: 112 °C
• Appearance: /
• Density: 1.052 g/cm³
• Vapor Pressure: 0.000966mmHg at 25°C
• Refractive Index: 1.53
• CAS DataBase Reference: 2-(ethylphenylamino)ethyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(ethylphenylamino)ethyl acetate(38954-40-4)
• EPA Substance Registry System: 2-(ethylphenylamino)ethyl acetate(38954-40-4)

Safety Data

• Hazardous Substances Data: 38954-40-4(Hazardous Substances Data)

Usage

General Description

2-(ethylphenylamino)ethyl acetate, also known as N-Ethyl-N-ethylaniline, is an organic compound with the chemical formula C12H17NO2. It is a clear, colorless liquid with a sweet, floral odor and is commonly used as a fragrance ingredient in perfumes, colognes, and other scented products. It is also used as a solvent and in the production of dyes and other chemicals. The compound is considered to have low toxicity, but it can cause irritation to the eyes, skin, and respiratory system upon contact. It should be handled with care and stored in a well-ventilated area away from heat and flame sources.

InChI:InChI=1/C12H17NO2/c1-3-13(9-10-15-11(2)14)12-7-5-4-6-8-12/h4-8H,3,9-10H2,1-2H3

Upstream product

• 92-50-2 2-( N-ethylanilino)ethanol 
• 75-36-5 acetyl chloride 
• 108-24-7 acetic anhydride 

Downstream Products

• 100609-71-0 4-[N-ethyl-N-(2'-acetoxyethyl)amino]benzaldehyde 
• 926634-45-9 trans-2-[4-(N-ethyl-N-(2-hydroxyethyl)amino)styryl]thiophene-5-carboxaldehyde 
• 926634-42-6 trans-2-[4-(N-ethyl-N-(2-hydroxyethyl)amino)styryl]thiophene 
• 926634-43-7 trans-2-[4-(N-ethyl-N-(2-tert-butyldimethylsiloxyethyl)amino)styryl]thiophene 
• 926634-44-8 trans-2-[4-(N-ethyl-N-(2-tert-butyldimethylsiloxyethyl)amino)styryl]thiophene-5-carboxaldehyde 
• 63619-28-3 4-(N-ethyl-N-(2-hydroxyethyl)amino)benzaldehyde 
• 122258-56-4 2-(ethyl(4-(2-(4-nitrophenyl)ethenyl)phenyl)amino)ethanol 
• 52239-04-0 C_.I_. Disperse Blue 148 
• 790240-34-5 3-[4-[N-ethyl-N-(2-tert-butyldimethylsiloxyethyl)amino]styryl]-5,5-dimethylcyclohex-2-enone 
• 790240-32-3 (E)-3-[4-[N-ethyl-N-(2-hydroxyethyl)amino]styryl]-5,5-dimethylcyclohex-2-enone 

Relevant articles and documents

Detection of explosive vapors with a charge transfer molecule: Self-assembly assisted morphology tuning and enhancement in sensing efficiency

Use of a fluorescent organic molecule consisting of binaphthyl functionalized with donor-acceptor substituted stilbenes for the detection of dinitrotoluene (DNT) and trinitrotoluene (TNT) vapors and enhancement in its sensing efficiency via self-assembly assisted morphology tuning are described. The Royal Society of Chemistry 2010.

Synthesis of a thiophene-based nonlinear optical chromophore

This report details an eight-step synthesis of the thiophene-type nonlinear optical chromophore 1 in 38% overall yield. Only one early step required chromatography. Copyright Taylor & Francis Group, LLC.

Image-formation material and infrared absorber

A heat mode-applicable image-formation material having high sensitivity and excellent image-forming property, and a novel infrared absorber which can be suitably used in this material. The present invention relates to a substrate carrying thereon an image-formation layer which contains an infrared absorption agent. The agent has at least one surface orientation group in the molecule, and solubility of the image-formation layer in an alkaline aqueous solution is changed by action of radiation in the near-infrared range. Preferable as the infrared absorbing agent is an infrared absorber comprising, in a molecule thereof, a fluorine-containing substituent which have at least 5 fluorine atoms, or a polymethine chain of at least 5 carbon atoms and an alkyl group of at least 8 carbon atoms, said alkyl group being connected to the polymethine chain via any of nitrogen, oxygen and sulfur.