6903-92-0

Basic information

• Product Name: 1H-Pyrrole-2,5-dione, 3-chloro-1-phenyl-4-(phenylamino)-
• Synonyms: 1H-Pyrrole-2,5-dione, 3-chloro-1-phenyl-4-(phenylamino)-
• CAS NO: 6903-92-0
• Molecular Formula: C₁₆H₁₁ClN₂O₂
• Molecular Weight: 298.72374
• Mol File: 6903-92-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Pyrrole-2,5-dione, 3-chloro-1-phenyl-4-(phenylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-2,5-dione, 3-chloro-1-phenyl-4-(phenylamino)-(6903-92-0)
• EPA Substance Registry System: 1H-Pyrrole-2,5-dione, 3-chloro-1-phenyl-4-(phenylamino)-(6903-92-0)

Safety Data

• Hazardous Substances Data: 6903-92-0(Hazardous Substances Data)

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.

Upstream product

• 1122-17-4 dichloromaleic acid anhydride 
• 62-53-3 aniline 
• 3876-05-9 3,4-dichloro-1-phenyl-1H-pyrrole-2,5-dione 
• 941-69-5 N-phenyl-maleimide 

Downstream Products

• 64094-05-9 3-anilino-4-morpholin-4-yl-1-phenyl-pyrrole-2,5-dione 
• 64093-94-3 morpholine-4-carbodithioic acid 4-anilino-2,5-dioxo-1-phenyl-2,5-dihydro-pyrrol-3-yl ester 
• 76039-46-8 3-Amino-1-phenyl-4-phenylamino-pyrrole-2,5-dione 
• 37648-47-8 2-phenyl-pyrrolo[3,4-b]quinoxaline-1,3-dione 
• 19035-04-2 N,N'-bis<(S)-1-phenylethyl>carbodiimide 
• 37648-63-8 N-phenylquinoxaline-2-carboxamide 
• 76039-52-6 3-Phenylcarbamoyl-quinoxaline-2-carboxylic acid; compound with ammonia 

Relevant articles and documents

Syntheses and structures of N-phenylmaleimidetriazoles and by-products

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

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.