14255-79-9

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

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

Relevant academic research and scientific papers

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

Synthesis, characterization, and antibacterial activity of some thiazoles derived from allyl thioureas

Synthesis of thiazoles was carried out from allyl thioureas using different cyclizing agents such as hydrogen chloride gas and bromine. Synthesized compounds were characterized by IR, 1H and 13C NMR, mass spectrometry, and elemental analysis. The synthesized thiazoles were evaluated for their antibacterial activity against Gram postitive (Lactobacillus bulgaris and Streptococcus mitis) and Gram negative (Yersinia) as well as antifungal activity against Aspergillus niger fungi.

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

Enzymatic Oxidative Conversion of Thio to Oxo by Baker's Yeast in Thiocarbamates and Thioureas

The enzymatic conversion of aryl allylthiocarbamates and 1-allyl-3-arylthioureas by baker's yeast to the corresponding carbamates and ureas in good yields is described.