5352-88-5

Basic information

• Product Name: N-(4-Chlorophenyl)-N'-methylurea
• Synonyms: Monomethylmonuron;N-(4-Chlorophenyl)-N'-methylurea;p-CPMU;1-(4-chlorophenyl)-3-Methylurea
• CAS NO: 5352-88-5
• Molecular Formula: C₈H₉ClN₂O
• Molecular Weight: 184.62
• Mol File: 5352-88-5.mol
• Article Data: 8

Chemical Properties

• Melting Point: 200 °C
• Boiling Point: 265.3°C at 760 mmHg
• Flash Point: 114.3°C
• Appearance: /
• Density: 1.288g/cm³
• Vapor Pressure: 0.00922mmHg at 25°C
• Refractive Index: 1.599
• PKA: 14.01±0.46(Predicted)
• CAS DataBase Reference: N-(4-Chlorophenyl)-N'-methylurea(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-Chlorophenyl)-N'-methylurea(5352-88-5)
• EPA Substance Registry System: N-(4-Chlorophenyl)-N'-methylurea(5352-88-5)

Safety Data

• Hazardous Substances Data: 5352-88-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C8H9ClN2O/c1-10-8(12)11-7-4-2-6(9)3-5-7/h2-5H,1H3,(H2,10,11,12)

Upstream product

• 104-12-1 p-chlorphenylisocyanate 
• 873-73-4 4-n-chlorophenylacetylene 
• 106-47-8 4-chloro-aniline 
• 598-50-5 N-Methylurea 
• 120-82-1 1,2,4-Trichlorobenzene 
• 372-09-8 cyanoacetic acid 
• 74-89-5 methylamine 
• 150-68-5 monuron 
• 25546-06-9 N'-(4-chloro-phenyl)-N-formyl-N-methyl-urea 
• 624-83-9 methyl isocyanate 
• 13256-32-1 1,3 dimethyl 1 nitrosourea 

Downstream Products

• 36744-17-9 3-(4-chloro-phenyl)-5-methyl-[1,3,5]thiadiazinan-4-one 
• 25355-61-7 1-(4-chlorophenyl)-3-isopropyl-3-nitrosourea 
• 31949-03-8 C₉H₈Cl₂N₂O₂ 
• 110396-88-8 C₈H₈ClN₃O₂ 
• 126381-33-7 3-(4-Chloro-phenyl)-1-(2-cyano-acetyl)-1-methyl-urea 
• 116571-28-9 1-(4-Chloro-phenyl)-3-methyl-imidazolidine-2,4,5-trione 
• 126381-39-3 6-Amino-1-(4-chloro-phenyl)-3-methyl-5-nitroso-1H-pyrimidine-2,4-dione 
• 7629-18-7 6-amino-1-(4-chloro-phenyl)-3-methyl-1H-pyrimidine-2,4-dione 
• 110396-85-5 isoamyl 4-chlorophenylcarbamate 
• 36743-37-0 3-(4-chloro-phenyl)-5-methyl-1,1-dioxo-1λ⁶-[1,3,5]thiadiazinan-4-one 
• 36744-20-4 3-(4-chloro-phenyl)-5-methyl-1-oxo-1λ⁴-[1,3,5]thiadiazinan-4-one 

Relevant articles and documents

Splitting a Substrate into Three Parts: Gold-Catalyzed Nitrogenation of Alkynes by C-C and C≡C Bond Cleavage

A gold-catalyzed nitrogenation of alkynes for the synthesis of carbamides and amino tetrazoles through C-C and C≡C bond cleavages is described. A diverse set of functionalized carbamide and amino tetrazole derivatives were selectively constructed under mild conditions. The chemoselectivity can be easily switched by the selection of the acid additives. The reaction is characterized by its broad substrate scope, direct construction of high value products, easy operation under air, and mild conditions at room temperature. This chemistry provides a way to transform alkynes by splitting the substrate into three parts.

Mineralisation of Monuron photoinduced by Fe(III) in aqueous solution

The degradation of Monuron (3-(4-chlorophenyl)-1,1-dimethylurea) photoinduced by Fe(III) in aqueous solution has been investigated. The rate of degradation depends on the concentration of Fe(OH)2+, the most photoreactive species in terms of su

Process for the preparation of pure, unsymmetrically disubstituted ureas

Process for the preparation of pure, unsymmetrically disubstituted ureas of the general formula STR1 in which R denotes a phenyl radical which is unsubstituted, or monosubstituted or polysubstituted by halogen atoms or alkyl, alkoxy, aryloxy or trifluoromethyl groups, an oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, benzoxazolyl or benzothiazolyl radical which is unsubstituted, or monosubstituted or polysubstituted by halogen atoms or alkyl, alkoxy or trifluoromethyl groups and R1 and R2 independently of one another denote a hydrogen atom or an alkyl group, where R1 and R2 are not simultaneously hydrogen or R1 and R2 together denote a butylene or pentylene group, by reaction of an N-alkyl- or N,N-dialkylurea with an unsubstituted or substituted arylamine or a heterocyclic amine in the presence of that amine which is already present in the starting material, the respective N-alkyl- or N,N-dialkylurea.