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Chemical compound
Diethylaniline is the organic compound with the molecular formula (C2H5)2NC6H5. It is a colorless liquid but commercial samples are often yellow. It is
Diethylaniline
Index of chemical compounds with the same molecular formula
C10H15N (molar mass: 149.23 g/mol, exact mass: 149.1204 u) may refer to: Diethylaniline, reducing agent/acid-absorbing base N,N-Dimethylphenethylamine, flavoring
C10H15N
Chemical compound
synthesised through a sequence characteristic of triphenylmethane dyes. Diethylaniline is first condensed with benzaldehyde, producing 4,4′-Bis(diethylamino)triphenylmethane
Brilliant_green_(dye)
Chemical compound
with borane-tetrahydrofuran (THF), borane-dimethylsulfide, borane-N,N-diethylaniline, or diborane as the borane source. Enantioselective reduction using
(R)-2-Methyl-CBS-oxazaborolidine
(R)-2-Methyl-CBS-oxazaborolidine
Chemical compound and chemical warfare nerve agent
The Aum Shinrikyo cult experimented with triethylamine as well. N,N-Diethylaniline was used by Aum Shinrikyo for acid reduction. Ammonia gas was used by
Sarin
Chemical compound
Concern since 2013. DHHB is produced by a reaction between 3-hydroxy-N,N-diethylaniline and phthalic anhydride, followed by esterification with 1-hexanol. DHHB
Diethylamino hydroxybenzoyl hexyl benzoate
Diethylamino_hydroxybenzoyl_hexyl_benzoate
Chemical compound and chemical warfare nerve agent
N-dimethylaminoethanol. The B in the following diagram denotes a base with diethylaniline being described as a suitable one in literature. Pampalakis, Georgios;
EA-1699
Chemical compound
Organic Letters. 10 (15): 3271–3273. doi:10.1021/ol8011502. "Role of Diethylaniline in the Reduction of 1,3-Dicarbonyl Compounds". Synfacts. 2009 (07):
Estrone_methyl_ether
Chemical compound
quaternary ammonium salt: C6H5N(CH3)2 +(CH3O)2SO2 → C6H5N(CH3)3CH3OSO3 Diethylaniline and dimethylaniline are both used as acid-absorbing bases. DMA is a
Dimethylaniline
(including C2-C12 homologues) UN 2431 6.1 Anisidines UN 2432 6.1 N,N-Diethylaniline UN 2433 6.1 Chloronitrotoluenes liquid or Chloronitrotoluenes solid
List of UN numbers 2401 to 2500
List_of_UN_numbers_2401_to_2500
Triarylmethane dye
chemist Heinrich Caro at BASF. Kern also found that by starting with diethylaniline rather than dimethylaniline, he could synthesize the closely related
Crystal_violet
Gunshot residue
ethylphenylcarbamyl chloride with monoethylaniline at 130 °C (266 °F) and by heating diethylaniline with phosgene under pressure. Ethyl centralite acts as a stabilizer
Centralite
Chemical reaction
using in situ prepared N,N-diethylaniline-borane and oxazaborolidine catalyst from sodium borohydride, N,N-diethylaniline hydrochloride and (S)-α,α-diphenylprolinol
Corey–Itsuno_reduction
Chemical synthesis
inverse-electron-demand Diels–Alder reaction of cyclophane 1 by heating in N,N-diethylaniline, with N2 gas being released as a byproduct to form compound 2. Chemoselective
Strychnine_total_synthesis
US EPA air pollutant emission standards
sulfate 121-69-7 N,N-Dimethylaniline Clean Air Act erroneously lists N,N-Diethylaniline 534-52-1 4,6-Dinitro-o-cresol, and salts 51-28-5 2,4-Dinitrophenol 121-14-2
National Emissions Standards for Hazardous Air Pollutants
National_Emissions_Standards_for_Hazardous_Air_Pollutants
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DIETHYLANILINE
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