6903-92-0 Usage
Chlorinated derivative
1-phenyl-4-(phenylamino)-1H-pyrrole-2,5-dione
The compound is modified by the addition of a chlorine atom to the base structure of 1-phenyl-4-(phenylamino)-1H-pyrrole-2,5-dione.
Application
Pesticide and herbicide in agriculture and horticulture
The chemical is used to control various pests and pathogens in agricultural and horticultural settings.
Mechanism of action
Inhibiting enzyme activity in target organisms
The compound works by inhibiting the activity of specific enzymes within the target organisms, which ultimately leads to their death.
Precaution
Potential hazards to human health and the environment
Care should be taken when handling the compound, as it may pose risks to both human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 6903-92-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,0 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6903-92:
(6*6)+(5*9)+(4*0)+(3*3)+(2*9)+(1*2)=110
110 % 10 = 0
So 6903-92-0 is a valid CAS Registry Number.
6903-92-0Relevant academic research and scientific papers
Syntheses and structures of N-phenylmaleimidetriazoles and by-products
Mao, Yingqun,Maley, Iain,Watson, William H.
, p. 385 - 403 (2007/10/03)
The syntheses, properties, and structures of N-phenylmaleimidetriazole derivatives are described. Intermediates and by-products are also discussed. 1b. a = 43.997(7) A, 5.7610(9) A, 8.245(1) A, β = 99.339(4)°, C2/c; 2a. a = 13.646(4) A, b = 7.7
Some synthetic applications of 2,3-dichloro-N-phenylmaleimide: A novel synthesis of 2-phenylpyrrolo[3,4-b]quinoxaline-1,3-diones. I
Hanaineh-Abdelnour, Leila,Bayyuk, Shibly,Theodorie, Rima
, p. 11859 - 11870 (2007/10/03)
2,3-Dichloro-N-phenylmaleimide 2 undergoes nucleophilic substitution reactions by a variety of nucleophiles giving either monosubstituted 5 or disubstituted 3 products. Treatment of 5 with sodium azide at room temperature results in cyclization to the corresponding 2-phenylpyrrolo[3,4- b]quinoxaline-1,3-diones 6, while at higher temperatures 5 is reduced to the 2-amino-amino-N-phenylmaleimides 7.
