25343-69-5

Basic information

• Product Name: 2,6-DIETHYLPHENYL ISOTHIOCYANATE
• Synonyms: 2,6-DIETHYLPHENYL ISOTHIOCYANATE;1,3-Diethyl-2-isothiocyanatobenzene;2,6-Diethylphenyl isothiocyate, 99%
• CAS NO: 25343-69-5
• Molecular Formula: C₁₁H₁₃NS
• Molecular Weight: 191.29
• EINECS: -0
• Mol File: 25343-69-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 130 °C
• Flash Point: 129-130°C/10mm
• Appearance: /
• Density: 1,03 g/cm3
• Vapor Pressure: 0.00176mmHg at 25°C
• Refractive Index: 1.6005
• Sensitive: Moisture Sensitive
• BRN: 2414870
• CAS DataBase Reference: 2,6-DIETHYLPHENYL ISOTHIOCYANATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DIETHYLPHENYL ISOTHIOCYANATE(25343-69-5)
• EPA Substance Registry System: 2,6-DIETHYLPHENYL ISOTHIOCYANATE(25343-69-5)

Safety Data

• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39
• RIDADR: 2810
• HazardClass: 6.1
• PackingGroup: II
• Hazardous Substances Data: 25343-69-5(Hazardous Substances Data)

Usage

General Description

2,6-Diethylphenyl isothiocyanate is a chemical compound with the molecular formula C11H13NS. It is a derivative of phenyl isothiocyanate, which is known for its strong and pungent odor. 2,6-Diethylphenyl isothiocyanate is used in organic synthesis as a reagent for the preparation of various compounds and as a starting material in the production of pesticides and pharmaceuticals. It is a colorless to pale yellow liquid with a boiling point of 243-245°C, and it is soluble in organic solvents such as ether and chloroform. As an isothiocyanate, it is known to have strong reactivity with nucleophiles, making it useful in a variety of chemical reactions. However, it is also important to note that isothiocyanates are known to be irritating to the skin, eyes, and respiratory tract and should be handled with caution and appropriate safety measures.

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

Downstream Products

• 68065-30-5 N-(2,6-Diaethylphenyl)-N'-methallylthioharnstoff 
• 1023254-39-8 1-(2,2-diethoxy-ethyl)-3-(2,6-diethyl-phenyl)-thiourea 
• 68065-29-2 N-(2,6-Diaethylphenyl)-N'-dodecylthioharnstoff 
• 66608-94-4 N-(2,6-diethyl-phenyl)-N'-sec.-butyl-thiourea 
• 1023039-43-1 C₁₉H₂₈N₂S 
• 1597614-70-4 (2,6-diethylphenyl)-(1-thia-3-aza-spiro[5.5]undec-2-en-2-yl)-amine 
• 88778-06-7 1-(2,6-diethylphenyl)-3-methylamidinothiourea 
• 69800-40-4 1-tert-Butyl-3-(2,6-diethyl-phenyl)-2-methyl-isothiourea 
• 487009-53-0 5-[(2,6-diethylanilino)(dimethylamino)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione 
• 487009-32-5 2,6-diethylphenyliminopropadienone 
• 439915-79-4 5-[(2,6-diethylanilino)(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione 
• 25372-34-3 1-(2,6-Diethyl-phenyl)-1H-imidazole-2-thiol 
• 25364-42-5 1-(2,6-diethylphenyl)-1H-imidazole 

Relevant articles and documents

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

A Facile, Modified Synthesis of Aryl Isothiocyanates from Methyl N-Aryldithiocarbamates

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