61874-13-3

Basic information

• Product Name: 2,6-Diethyl-N-(2-propoxyethyl)aniline
• Synonyms: 2,6-DIETHYL-N-(2-PROPOXYETHYL)ANILINE;2,6-Diethyl-N-(2-propoxyethyl)-benzenamine;N-Propoxyethyl-2,6-Diethyl Aniline
• CAS NO: 61874-13-3
• Molecular Formula: C15H25NO
• Molecular Weight: 235.37
• Mol File: 61874-13-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 352°C
• Flash Point: 150°C
• Appearance: light yellow transparent liquid
• Density: 0.953
• Vapor Pressure: 4.04E-05mmHg at 25°C
• Refractive Index: 1.521
• PKA: 4.01±0.50(Predicted)
• CAS DataBase Reference: 2,6-Diethyl-N-(2-propoxyethyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Diethyl-N-(2-propoxyethyl)aniline(61874-13-3)
• EPA Substance Registry System: 2,6-Diethyl-N-(2-propoxyethyl)aniline(61874-13-3)

Safety Data

• Hazardous Substances Data: 61874-13-3(Hazardous Substances Data)

Usage

General Description

2,6-Diethyl-N-(2-propoxyethyl)aniline is a complex organic chemical compound that is a part of the larger aniline family, often used in various industries. In its pure form, it is generally a light yellow liquid that does not readily dissolve in water but is soluble in most organic solvents, including toluene and benzene. The main use of 2,6-Diethyl-N-(2-propoxyethyl)aniline is as a key intermediate in the production of dyes, particularly those used in textile industries, as well as various pigments, and it can also be used in the manufacture of drugs and agrochemicals. Due to its potential toxicity and flammability, careful handling and specific regulations are required when working with this chemical.

InChI:InChI=1/C15H25NO/c1-4-11-17-12-10-16-15-13(5-2)8-7-9-14(15)6-3/h7-9,16H,4-6,10-12H2,1-3H3

Upstream product

• 56680-69-4 2-n-propoxyacetyl chloride 
• 579-66-8 2,6-diethylaniline 
• 42149-74-6 2-chloroethyl propyl ether 
• 19790-53-5 3-propoxypropionaldehyde 

Relevant articles and documents

Construction and Characterization of 3,7-Dichloro-N-(2,6-Diethylphenyl)-N-(2-Propoxyethyl)Quinolone-8-Carboxamide: A Potential Novel Pesticide Compound

[Figure not available: see fulltext.] A novel compound, 3,7-dichloro-N-(2,6-diethylphenyl)-N-(2-propoxyethyl)quinoline-8-carboxamide was synthesized by splicing together a chloro-substituted quinoline moiety found in quinclorac (a selective herbicide) and a substituted amide moiety found in pretilachlor (another selective herbicide) using the active substructure splicing method. The chemical structure of this compound was characterized by 1H, 13C NMR, FTIR, high-resolution mass spectra and X-ray diffraction analysis. Pesticide potency (herbicidal and fungicidal activity) of this compound was evaluated. This compound displayed excellent control efficiency against Echinochloa crusgalli and also showed good fungicidal in vitro activity against Phytophthora capsici, Phytophthora sojae, and Phytophthora infestans.

Pretilachlor synthesis method

The invention discloses a pretilachlor synthesis method. The pretilachlor synthesis method comprises steps as follows: sodium propanolate is dissolved in an organic solvent I, 2-chloroacetaldehyde dimethyl acetal is added dropwise, and heat is preserved until the reaction is performed completely; propoxy acetaldehyde dimethyl acetal and tetrahydrofuran are mixed, aqueous acid is added, and heat is preserved until the reaction is performed completely; 3-propoxy propionaldehyde, 2,6-diethyl aniline and an organic solvent II are mixed, a catalyst is added, hydrogen is introduced until certain pressure is obtained, and heat is preserved until the reaction is performed completely; amidogen ether, a sodium hydroxide solution and methylbenzene are mixed, chloroacetyl chloride is added dropwise at certain temperature, heat is preserved until the reaction is performed completely, and pretilachlor is prepared. With the adoption of the method, high-quality pretilachlor can be obtained.