5428-50-2

Usage

Uses

Used in Agricultural Industry:
1-(2,4-DICHLOROPHENYL)UREA is used as a plant morphogenesis regulator and crop immunomodulator for enhancing plant growth, development, and resistance to various stress factors. It helps in controlling the growth patterns of plants, promoting uniformity, and increasing crop yield. Additionally, it acts as an immunomodulator, strengthening the plants' defense mechanisms against pests and diseases, thereby reducing the need for chemical pesticides and contributing to sustainable agriculture.
Used in Chemical Synthesis:
1-(2,4-DICHLOROPHENYL)UREA serves as a key intermediate in the synthesis of various chemical compounds, such as [(Furyl)butyl]dichlorophenylurea. This synthesized compound finds applications in the agricultural industry as a plant growth regulator and immunomodulator, further expanding the utility of 1-(2,4-DICHLOROPHENYL)UREA in developing innovative solutions for agricultural challenges.

InChI:InChI=1/C7H6Cl2N2O/c8-4-1-2-6(5(9)3-4)11-7(10)12/h1-3H,(H3,10,11,12)

Upstream product

• 64-10-8 phenyl carbamate 
• 7782-50-5 chlorine 
• 64-19-7 acetic acid 
• 29084-76-2 2,4-dichloroaniline hydrochloride 
• 57-13-6 urea 
• 6326-14-3 2,4-dichlorophenylthiourea 

Downstream Products

• 872265-83-3 N-chloro-N'-(2,4,6-trichloro-phenyl)-urea 
• 732223-04-0 N-(2,4-dichlorophenyl)hydrazinecarboxamide 
• 136757-14-7 (2,4,6-trichloro-phenyl)-urea 
• 872265-82-2 N,N-dichloro-N'-(2,4-dichloro-phenyl)-urea 

Relevant academic research and scientific papers

Novel synthesis and biological evaluations of N,N’-disubstituted-3,6-bis(substitutedphenyl)-1,2,4,5-tetrazine-1,4-dicarboxamide

A series of novel N,N’-disubstituted-3,6-bis(substitutedphenyl) -1,2,4,5-tetrazine-1,4-dicarboxamides were prepared using the intermolecular cyclization reaction of N-substituted-N’-(α-chloro-substitutedbenzylidene) hydrazinecarboxamide and triethylamine by the modification of solvent polarity. The structures of all the new compounds were characterized by IR, 1H-NMR, MS and elemental analysis. Their cytostatic effects were screened in vitro by the SRB method for A-549 cell and the MTT method for P-388 cell. The results showed that several compounds demonstrate potential antitumor activities against P-388. The substituents have clearly effect on their antitumor activity.

Selective and facile oxidative desulfurization of thioureas and thiobarbituric acids with singlet molecular oxygen generated from trans-3,5-dihydroperoxy-3,5-dimethyl-1,2-dioxolane

An efficient and facile procedure using trans-3,5-dihydroperoxy-3,5-dimethyl-1,2-dioxolane has been developed for oxidative desulfurization of thioureas and thiobarbituric acids. The reactions proceeded smoothly very fast under mild conditions in basic media at room temperature to afford the respective ureas in excellent yields. Simple procedure and work up, mild conditions, high yields, short reaction times, use of highly potent and non-toxic oxidant are the main merits of the present method.