2828-42-4 Usage
Uses
Used in Agriculture:
PROXIMPHAM is used as a herbicidal agent for the control of broadleaf weeds and grasses in various crops. It is particularly effective in soybeans, cotton, and peanuts, ensuring their healthy growth by eliminating competing vegetation.
PROXIMPHAM is used as a selective herbicide for the following reasons:
It inhibits the synthesis of specific enzymes essential for plant growth, disrupting the cellular processes of unwanted plants and leading to their death.
It has low toxicity to mammals, making it a safer option for agricultural use.
It is relatively stable in the environment, reducing the potential for long-term ecological impact.
By following the appropriate safety guidelines and regulations, PROXIMPHAM can be effectively utilized to enhance crop yields and maintain the productivity of agricultural lands.
Check Digit Verification of cas no
The CAS Registry Mumber 2828-42-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,2 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2828-42:
(6*2)+(5*8)+(4*2)+(3*8)+(2*4)+(1*2)=94
94 % 10 = 4
So 2828-42-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O2/c1-8(2)12-14-10(13)11-9-6-4-3-5-7-9/h3-7H,1-2H3,(H,11,13)
2828-42-4Relevant academic research and scientific papers
Reactivity of bis(arylcarbamoyl)-N-arylphenacylamine oximes. Synthesis of 1,3-dihydroimidazol-2-ones and N-unsubstituted O- arylcarbamoylhydroxylamines
Coskun, Necdet
, p. 475 - 484 (2007/10/03)
N-Arylphenacylamine oximes 1 reacted with aryl isocyanates in refluxing benzene to give bis(arylcarbamoyl)-N-arylphenacylamine oximes 2 in good yields. Compounds 2 reacted with equimolar amount of TsOH.H2O in THF at room temperature to give imidazol-2-ones 5 and O-arylcarbamoylhydroxylammonium tosylates 6 in high yields. Compounds 2 were heated under vacuum to induce Beckmann fragmentation but the resulting products were 1,3,4-triaryl-1,3- dihydroimidazol-2-ones 5 instead of the expected 1,3-diazetidinones 4.
