217487-17-7

Basic information

• Product Name: 3-(4-isopropylphenyl)-1,1-dimethylurea-d6
• Synonyms: isoproturon d6 (dimethyl d6)
• CAS NO: 217487-17-7
• Molecular Formula: C12H12D6N2O
• Molecular Weight: 0
• Mol File: 217487-17-7.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 353.2°C at 760 mmHg
• Flash Point: 167.4°C
• Appearance: /
• Density: 1.081g/cm³
• Vapor Pressure: 3.64E-05mmHg at 25°C
• Refractive Index: 1.555
• CAS DataBase Reference: 3-(4-isopropylphenyl)-1,1-dimethylurea-d6(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-isopropylphenyl)-1,1-dimethylurea-d6(217487-17-7)
• EPA Substance Registry System: 3-(4-isopropylphenyl)-1,1-dimethylurea-d6(217487-17-7)

Safety Data

• Hazard Codes: Xn,N
• Statements: 40-50/53
• Safety Statements: 36/37-60-61
• RIDADR: UN 3077 9/PG 3
• WGK Germany: 3
• Hazardous Substances Data: 217487-17-7(Hazardous Substances Data)

Usage

Description

3-(4-isopropylphenyl)-1,1-dimethylurea-d6, also known as Isoproturon-d6, is a deuterated or labeled form of Isoproturon (I874500). It is a chemical compound that has been modified by the addition of deuterium atoms, which are isotopes of hydrogen. This modification can enhance the stability and solubility of the compound, making it more suitable for certain applications.

Uses

Used in Agricultural Industry:
Isoproturon-d6 is used as a pre-and post-emergence herbicide for the control of annual grasses and broad-leaved weeds. It is particularly effective in managing unwanted plant growth in agricultural settings, helping to protect crops and improve overall yield.
Used in Research and Development:
Isoproturon-d6 is also utilized in research and development for various applications. The deuterated form of the compound can be used to study the effects of isotopic substitution on chemical reactions and to investigate the behavior of the molecule in different environments. This can provide valuable insights into the properties and potential uses of the compound, as well as contribute to the development of new and improved products.
Used in Environmental Monitoring:
In addition to its agricultural applications, Isoproturon-d6 can be employed in environmental monitoring to track the presence and distribution of the compound in the environment. This can help to assess the potential impact of Isoproturon on ecosystems and to develop strategies for its safe and effective use.
Used in Pharmaceutical Industry:
Isoproturon-d6 may also have potential applications in the pharmaceutical industry, where it could be used as a starting material for the synthesis of new drugs or as a tool for studying the interactions between molecules and biological targets. The deuterated form of the compound can provide valuable information about the structure and function of these targets, leading to the development of more effective and targeted therapies.

InChI:InChI=1/C12H18N2O/c1-9(2)10-5-7-11(8-6-10)13-12(15)14(3)4/h5-9H,1-4H3,(H,13,15)/i3D3,4D3

Upstream product

• 31027-31-3 4-isopropylphenylisocyanate 
• 124-40-3 dimethyl amine 
• 366-18-7 [2,2]bipyridinyl 
• 1817-47-6 4-nitrocumene 
• 99-88-7 4-Isopropylaniline 
• 79-44-7 N,N-Dimethylcarbamoyl chloride 
• 506-59-2 N,N-dimethylammonium chloride 
• 124-38-9 carbon dioxide 
• 56046-17-4 3-[4-(1-methylethyl)]phenylurea 

Downstream Products

• 38652-14-1 1-(4-hydroxyphenyl)-3-methylurea 

Relevant articles and documents

2,2,2-Trifluroenthanol promoted synthesis of unsymmetrical ureas from dioxazolones and amines via tandem lossen rearrangement/condensation process

A 2,2,2-trifluroenthanol (TFE) promoted synthesis of unsymmetric ureas was described. This approach enabled the construction of a variety of ureas from the readily prepared and easy-to-handle dioxazolones and amines via tandem Lossen rearrangement/condensation process. The reaction featured mild conditions for the urea synthesis under metal-free conditions, which was successively applied in the scale-up synthesis of herbicides Monuro and Isoproturon.

A practically simple, catalyst free and scalable synthesis of: N -substituted ureas in water

A practically simple, mild and efficient method is developed for the synthesis of N-substituted ureas by nucleophilic addition of amines to potassium isocyanate in water without organic co-solvent. Using this methodology, a variety of N-substituted ureas (mono-, di- and cyclic-) were synthesized in good to excellent yields with high chemical purity by applying simple filtration or routine extraction procedures avoiding silica gel purification. The developed methodology was also found to be suitable for gram scale synthesis of molecules having commercial application in large volumes. The identified reaction conditions were found to promote a unique substrate selectivity from a mixture of two amines.

NOXIOUS ARTHROPOD CONTROL AGENT CONTAINING AMIDE COMPOUND

An object of the present invention is to provide a compound having the controlling activity on a noxious arthropod, and a noxious arthropod controlling agent containing an amide compound of formula (I): wherein X represents a nitrogen atom or a CH group, p represents 0 or 1, A represents a tetrahydrofuranyl group or the like, R1, R2, R3, R4, R5, R6 and R7 represent a hydrogen atom or the like, n represents 1 or 2, Y represents an oxygen atom or the like, m represents any integer of 0 to 7, and Q represents a C1-8 chain hydrocarbon group optionally having a phenyl group or the like, has the excellent noxious arthropod controlling effect.