25343-69-5

Usage

Uses

Used in Organic Synthesis:
2,6-DIETHYLPHENYL ISOTHIOCYANATE is used as a reagent in organic synthesis for the preparation of various compounds. Its strong reactivity with nucleophiles allows for the creation of a wide range of chemical products.
Used in Pesticide Production:
In the agricultural industry, 2,6-DIETHYLPHENYL ISOTHIOCYANATE is used as a starting material in the production of pesticides. Its chemical properties make it a valuable component in developing effective pest control agents.
Used in Pharmaceutical Industry:
2,6-DIETHYLPHENYL ISOTHIOCYANATE is also utilized as a starting material in the pharmaceutical industry for the development of new drugs. Its unique chemical structure contributes to the creation of potential therapeutic agents.

InChI:InChI=1/C11H13NS/c1-3-9-6-5-7-10(4-2)11(9)12-8-13/h5-7H,3-4H2,1-2H3

Upstream product

• 579-66-8 2,6-diethylaniline 
• 463-71-8 thiophosgene 
• 103-72-0 phenyl isothiocyanate 
• 85046-69-1 (2,6-Diethyl-phenyl)-dithiocarbamic acid methyl ester 

Downstream Products

• 68065-23-6 N-(2,6-Diaethylphenyl)-N'-propylthioharnstoff 
• 66608-94-4 N-(2,6-diethyl-phenyl)-N'-sec.-butyl-thiourea 
• 68065-29-2 N-(2,6-Diaethylphenyl)-N'-dodecylthioharnstoff 
• 66608-91-1 N-(2.6-Diaethyl-phenyl)-N'-tert.-pentyl-thioharnstoff 
• 68065-26-9 N-(2,6-Diaethylphenyl)-N'-neopentylthioharnstoff 
• 68065-27-0 N-(2,6-Diaethylphenyl)-N'-hexylthioharnstoff 
• 67330-74-9 1-(2,6-Diethyl-phenyl)-3-(1,2,2-trimethyl-propyl)-thiourea 
• 68065-21-4 N-(2,6-Diaethylphenyl)-N'-isobutylthioharnstoff 
• 68065-22-5 N-(2,6-Diaethylphenyl)-N'-aethylthioharnstoff 
• 24053-71-2 N¹.N¹-Dimethyl-N²-<2.6-diethyl-phenyl>-thioharnstoff 
• 66649-68-1 N-(2,6-diethyl-phenyl)-N'-isopropyl-thiourea 
• 66608-90-0 N-(2,6-diethyl-phenyl)-N'-tert.-butyl-thiourea 
• 68065-24-7 N-(2,6-Diaethylphenyl)-N'-butylthioharnstoff 
• 67330-72-7 1-(2,6-Diethyl-phenyl)-3-(1-methyl-butyl)-thiourea 

Relevant academic research and scientific papers

Optically active iridium imidazol-2-ylidene-oxazoline complexes: Preparation and use in asymmetric hydrogenation of arylalkenes

This work explores the potential of iridium complexes of the N-heterocyclic carbene oxazoline ligands 1 in asymmetric hydrogenations of arylalkenes. The accessible carbene precursors, imidazolium salts 2, and robust iridium complexes 5 facilitated a disco

Iminopropadienones from dioxanediones, isoxazolopyrimidinones, pyridopyrimidinones, and pyridopyrimidinium olates

Iminopropadienones, RN=C=C=C=O, can be generated from four different types of precursors in flash vacuum thermolysis reactions: 1,3-dioxane-4,6-diones 1, isoxazolopyrimidinones 2, pyridopyrimidinium olates 3, and pyridopyrimidinones 4. 2,6-Difluorophenyl-, 2,6-diethylphenyl-, o-tertbutylphenyl-, and mesityliminopropadienone have been directly observed by Ar matrix IR spectroscopy in one or more of these reactions. Reactions with bis-nucleophiles afford pyridopyrimidinones and perhydrodiazepinone derivatives.