3420-63-1

Basic information

• Product Name: 1-(3-chloropropyl)-3-phenylurea
• CAS NO: 3420-63-1
• Molecular Formula: C₁₀H₁₃ClN₂O
• Molecular Weight: 212.676
• Mol File: 3420-63-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 319.3°C at 760 mmHg
• Flash Point: 146.9°C
• Density: 1.21g/cm³
• Vapor Pressure: 0.000341mmHg at 25°C
• Refractive Index: 1.576
• CAS DataBase Reference: 1-(3-chloropropyl)-3-phenylurea(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-chloropropyl)-3-phenylurea(3420-63-1)
• EPA Substance Registry System: 1-(3-chloropropyl)-3-phenylurea(3420-63-1)

Safety Data

• Hazardous Substances Data: 3420-63-1(Hazardous Substances Data)

Usage

Type of compound

Organic compound

Derivative of

Urea

Contains

Phenyl group and 3-chloropropyl group

Application

Herbicide

Mechanism of action

Inhibits plant growth by interfering with protein synthesis

Usage

Control of weeds in agricultural settings

Classification

Selective herbicide

Physical state

Crystalline solid

Solubility

Sparingly soluble in water

Application methods

Spray or granule in agricultural fields

Upstream product

• 13010-19-0 3-Chloropropyl isocyanate 
• 62-53-3 aniline 
• 4635-59-0 4-Chlorobutanoyl chloride 

Downstream Products

• 1311946-15-2 2-tolyl 4-[tetrahydro-2-oxopyrimidin-1(2H)-yl]benzenesulfonate 
• 1311946-17-4 2-ethylphenyl 4-[tetrahydro-2-oxopyrimidin-1(2H)-yl]benzenesulfonate 
• 1311946-19-6 2-propylphenyl 4-[tetrahydro-2-oxopyrimidin-1(2H)-yl]benzenesulfonate 
• 1311946-20-9 2,4-dimethylphenyl 4-[tetrahydro-2-oxopyrimidin-1(2H)-yl]benzenesulfonate 
• 1311946-22-1 2,4,5-trichlorophenyl 4-[tetrahydro-2-oxopyrimidin-1(2H)-yl]benzenesulfonate 
• 1311946-24-3 2,4,6-trichlorophenyl 4-[tetrahydro-2-oxopyrimidin-1(2H)-yl]benzenesulfonate 
• 1311946-26-5 3-tolyl 4-[tetrahydro-2-oxopyrimidin-1(2H)-yl]benzenesulfonate 
• 1311946-27-6 3-methoxyphenyl 4-[tetrahydro-2-oxopyrimidin-1(2H)-yl]benzenesulfonate 
• 1311946-28-7 3-fluorophenyl 4-[tetrahydro-2-oxopyrimidin-1(2H)-yl]benzenesulfonate 
• 1311946-29-8 3,4,5-trimethoxyphenyl 4-[tetrahydro-2-oxopyrimidin-1(2H)-yl]benzenesulfonate 
• 1311946-30-1 4-tolyl 4-[tetrahydro-2-oxopyrimidin-1(2H)-yl]benzenesulfonate 
• 1311946-32-3 4-chlorophenyl 4-[tetrahydro-2-oxopyrimidin-1(2H)-yl]benzenesulfonate 
• 1311946-34-5 4-fluorophenyl 4-[tetrahydro-2-oxopyrimidin-1(2H)-yl]benzenesulfonate 
• 91180-81-3 1-Phenyl-3-methyl-3,4,5,6-tetrahydropyrimidin-2(1H)-one 

Relevant articles and documents

Design, synthesis, biological evaluation, and Structure - Activity relationships of substituted phenyl 4-(2-oxoimidazolidin-1-yl)benzenesulfonates as new tubulin inhibitors mimicking combretastatin A-4

Sixty-one phenyl 4-(2-oxoimidazolidin-1-yl)benzenesulfonates (PIB-SOs) and 13 of their tetrahydro-2-oxopyrimidin-1(2H)-yl analogues (PPB-SOs) were prepared and biologically evaluated. The antiproliferative activities of PIB-SOs on 16 cancer cell lines are

Cyclic ureas as ortho directing substituents

Six-membered cyclic ureas are shown to have a weak ortho directing ability when linked through nitrogen to benzene and pyridine rings.

The synthesis of potential anticancer agents. XXXVI. N-nitrosoureas. II. Haloalkyl derivatives.

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