14255-79-9

Basic information

• Product Name: 1-(4-chlorophenyl)-3-prop-2-en-1-ylthiourea
• Synonyms: 1-Allyl-3-(4-chlorophenyl)thiourea; thiourea, N-(4-chlorophenyl)-N'-2-propen-1-yl-
• CAS NO: 14255-79-9
• Molecular Formula: C₁₀H₁₁ClN₂S
• Molecular Weight: 226.7257
• Mol File: 14255-79-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 311.5°C at 760 mmHg
• Flash Point: 142.2°C
• Density: 1.264g/cm³
• Vapor Pressure: 0.00056mmHg at 25°C
• Refractive Index: 1.648
• CAS DataBase Reference: 1-(4-chlorophenyl)-3-prop-2-en-1-ylthiourea(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-chlorophenyl)-3-prop-2-en-1-ylthiourea(14255-79-9)
• EPA Substance Registry System: 1-(4-chlorophenyl)-3-prop-2-en-1-ylthiourea(14255-79-9)

Safety Data

• Hazardous Substances Data: 14255-79-9(Hazardous Substances Data)

Usage

Organochlorine compound

Derived from thiourea with a chlorine atom

Phenyl group substitution

At the 4-position

Prop-2-en-1-yl group substitution

At the 3-position

Chemical structure

Contains a thiourea functional group, a phenyl ring, and a prop-2-en-1-yl group

Synthesis

Commonly used in the synthesis of other organic compounds

Biological activities

Studied for antifungal and antiparasitic properties

Agricultural applications

Investigated as a potential pesticide

Pharmaceutical applications

Explored for potential medicinal uses

Versatility

Due to its molecular structure and properties, it has potential applications in various fields

Upstream product

• 106-47-8 4-chloro-aniline 
• 57-06-7 N-allyl isothiocyanate 

Downstream Products

• 51784-10-2 N-(2,3-dibromopropyl)isothiocyanate 
• 874-17-9 4-chloro-2,6-dibromoaniline 
• 1354377-95-9 2-[1-[3-allyl-2-[(4-chlorophenyl)imino]-4-oxo-1,3-thiazolidin-5-ylidene]ethyl]hydrazinecarboxamide 
• 1019333-98-2 C₁₆H₁₅ClN₂SSe 
• 37919-93-0 N-allyl-N'-(4-chlorophenyl)urea 
• 75220-48-3 N-(4-chlorophenyl)-5-methyl-4,5-dihydrothiazol-2-amine 
• 860574-47-6 N-acetyl-N'-allyl-N-(4-chloro-phenyl)-thiourea 

Relevant articles and documents

Synthesis of new thioureas derivatives and evaluation of their efficacy as proliferation inhibitors in mcf-7 breast cancer cells by using99m tc-mibi radiotracer

Background & Objective: Anti-tumor activity of some thioureas derivatives is well documented in literature and received considerable attention. The present study aims to synthesize and characterize some novel thioureas and carbonylthioureas as anti-tumor

Powerful approach to heterocyclic skeletal diversity by sequential three-component reaction of amines, isothiocyanates, and 1,2-diaza-1,3-dienes

By highly efficient, one-pot, three-component reactions, combining one set of 1,2-diaza-1,3-dienes (DDs), primary amines, and isothiocyanates in a different sequential order of addition, heterocyclic skeletal diversity can be achieved. The key feature dis