19095-82-0 Usage
General Description
1-cyclohexyl-3-(3-methylphenyl)urea is a chemical compound that belongs to the class of urea derivatives. It is also known by the trade name "Cycluradam." 1-cyclohexyl-3-(3-methylphenyl)urea is commonly used as a pesticide, particularly as an insecticide and acaricide, to control a variety of pests in agriculture. It works by interfering with the pests' physiological and biochemical processes, ultimately leading to their death. 1-cyclohexyl-3-(3-methylphenyl)urea is known for its efficacy in controlling a wide range of insects and mites while posing minimal risk to non-target organisms and the environment. Additionally, it has low water solubility, which makes it less likely to leach into groundwater. Overall, this chemical compound plays a crucial role in pest management and crop protection in the agricultural industry.
Check Digit Verification of cas no
The CAS Registry Mumber 19095-82-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,9 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19095-82:
(7*1)+(6*9)+(5*0)+(4*9)+(3*5)+(2*8)+(1*2)=130
130 % 10 = 0
So 19095-82-0 is a valid CAS Registry Number.
19095-82-0Relevant articles and documents
Z-Selective Fluoroalkenylation of (Hetero)Aromatic Systems by Iodonium Reagents in Palladium-Catalyzed Directed C?H Activation
Tóth, Balázs L.,Sályi, Gerg?,Domján, Attila,Egyed, Orsolya,Bényei, Attila,Gonda, Zsombor,Novák, Zoltán
supporting information, p. 348 - 354 (2021/11/09)
The direct and catalytic incorporation of fluorine containing molecular motifs into organic compounds resulting high-value added chemicals represents a rapidly evolving part of synthetic methodologies, thus this area is in the focus of pharmaceutical and agrochemical research. Herein we report a stereoselective procedure for direct fluorovinylation of aromatic and heteroaromatic scaffolds. This methodology development has been realized by palladium-catalyzed ortho C?H activation reaction of aniline derivatives featuring the regioselectivity via directing groups such as secondary of tertiary amides, ureas or ketones. The application of non-symmetrical aryl(fluoroalkenyl)-iodonium salts as fluoroalkenylating agents allowed mild reaction conditions in general for this transformation. The scope and limitations have been thoroughly investigated and the feasibility has been demonstrated by more than 50 examples.