5428-50-2

Basic information

• Product Name: 1-(2,4-DICHLOROPHENYL)UREA
• Synonyms: 1-(2,4-DICHLOROPHENYL)UREA;linuron impurity
• CAS NO: 5428-50-2
• Molecular Formula: C₇H₆Cl₂N₂O
• Molecular Weight: 205.04
• Mol File: 5428-50-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 296°Cat760mmHg
• Flash Point: 132.8°C
• Appearance: /
• Density: 1.534g/cm³
• Vapor Pressure: 0.00147mmHg at 25°C
• Refractive Index: 1.658
• Storage Temp.: Refrigerator, Under inert atmosphere
• Solubility: Chloroform (Slightly, Heated, Sonicated), DMSO (Slightly)
• CAS DataBase Reference: 1-(2,4-DICHLOROPHENYL)UREA(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,4-DICHLOROPHENYL)UREA(5428-50-2)
• EPA Substance Registry System: 1-(2,4-DICHLOROPHENYL)UREA(5428-50-2)

Safety Data

• Hazardous Substances Data: 5428-50-2(Hazardous Substances Data)

Usage

Uses

N-(2,4-Dichlorophenyl)urea is used in preparation of [(Furyl)butyl]dichlorophenylurea as plant morphogenesis regulator and crop immunomodulator.

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

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

Relevant articles and documents

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.