2827-18-1

Basic information

• Product Name: 1-ethyl-3-(4-methylphenyl)thiourea
• Synonyms: 1-Ethyl-3-(4-methylphenyl)thiourea; thiourea, N-ethyl-N'-(4-methylphenyl)-
• CAS NO: 2827-18-1
• Molecular Formula: C₁₀H₁₄N₂S
• Molecular Weight: 194.2966
• Mol File: 2827-18-1.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 283°C at 760 mmHg
• Flash Point: 125°C
• Density: 1.129g/cm³
• Vapor Pressure: 0.00325mmHg at 25°C
• Refractive Index: 1.625
• CAS DataBase Reference: 1-ethyl-3-(4-methylphenyl)thiourea(CAS DataBase Reference)
• NIST Chemistry Reference: 1-ethyl-3-(4-methylphenyl)thiourea(2827-18-1)
• EPA Substance Registry System: 1-ethyl-3-(4-methylphenyl)thiourea(2827-18-1)

Safety Data

• Hazardous Substances Data: 2827-18-1(Hazardous Substances Data)

Usage

General Description

1-Ethyl-3-(4-methylphenyl)thiourea is a chemical compound with the formula C11H16N2S. It is a thiourea derivative, which is a class of compounds known for their diverse biological and industrial applications. This specific compound is used as a fungicide and is known for its ability to inhibit the growth of various types of fungi. It is also used in the development of pharmaceuticals and as a reagent in organic synthesis. 1-Ethyl-3-(4-methylphenyl)thiourea has been studied for its potential therapeutic applications, particularly in the treatment of parasitic infections and as an anti-tumor agent. It is important to handle this compound with care, as it may pose risks to human health and the environment if not properly managed and disposed of.

Upstream product

• 75-04-7 ethylamine 
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• 542-85-8 Ethyl isothiocyanate 
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Downstream Products

• 61449-47-6 2,4-diethyl-3,5-bis(4-methylphenylimino)-1,2,4-thiadiazolidine 
• 1170007-04-1 1-ethyl-2-isopropyl-3-p-tolylisothiourea 
• 1096570-88-5 C₂₄H₂₂N₂S 
• 1096570-85-2 C₁₉H₂₀N₂S 
• 55695-44-8 (3-amino-4-p-tolyl-4H-[1,2,4]thiadiazol-5-ylidene)-ethyl-amine 
• 85063-61-2 N-ethyl-6-methylbenzo[d]thiazol-2-amine 

Relevant articles and documents

Synthesis, characterization and structural study of new ethyl thiourea compounds and the preliminary naked-eye sensors for mercury and argentum metal ions

Novel ethyl thiourea compounds 1a- 1f have been synthesized in good to high yields. The structure of all compounds were identified using FT-IR, 1H NMR, 13C NMR spectroscopies, and ESI-Mass spectrometry. The compound 1-ethyl-3-(3-meth

Synthesis of thiazolidines via regioselective addition of unsymmetric thioureas to maleic acid derivatives

A wide range of unsymmetric thioureas has been studied in reaction with N-arylmaleimides and maleic anhydride. The regioselectivity of the addition depends not only on steric factors but on both solvent polarity and type of maleic acid derivative (imide o

A convenient one-pot three component approach to synthesis of highly substituted iminothiazolines

An efficient one-pot three component method was developed for the synthesis of highly substituted 2-iminothizolines by the reaction of isothiocyanates, primary amines and α-bromoketones in ambient temperature. The reaction produced the desired products in a completely regioselective manner in excellent yields (78-94%). The Japan Institute of Heterocyclic Chemistry.