160984-02-1

Basic information

• Product Name: N-(2-fluoro-4-nitrophenyl)-1-cyclohexene-1,2-dicarboximide
• Synonyms: N-(2-fluoro-4-nitrophenyl)-1-cyclohexene-1,2-dicarboximide
• CAS NO: 160984-02-1
• Molecular Weight: 290.251
• Mol File: 160984-02-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(2-fluoro-4-nitrophenyl)-1-cyclohexene-1,2-dicarboximide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-fluoro-4-nitrophenyl)-1-cyclohexene-1,2-dicarboximide(160984-02-1)
• EPA Substance Registry System: N-(2-fluoro-4-nitrophenyl)-1-cyclohexene-1,2-dicarboximide(160984-02-1)

Safety Data

• Hazardous Substances Data: 160984-02-1(Hazardous Substances Data)

Upstream product

• 2426-02-0 3,4,5,6-Tetrahydrophthalic anhydride 
• 369-35-7 2-fluoro-4-nitroaniline 
• 348-19-6 2'-fluoro-4'-nitroacetanilide 
• 399-31-5 N-(2-fluorophenyl)acetamide 
• 402-67-5 3-fluoro-1-nitrobenzene 
• 348-54-9 2-Fluoroaniline 

Downstream Products

• 160984-03-2 N-(4-amino-2-fluorophenyl)-1-cyclohexene-1,2-dicarboximide 

Relevant articles and documents

Preparation and alkylation of regioisomeric tetrahydrophthalimide-substituted indolin-2(3H)-ones

A series of novel regioisomeric tetrahydrophthalimide-substituted indolin-2-ones has been prepared via the Sommelet-Hauser type cyclization of appropriately substituted anilines as potential herbicides. The resultant indolin-2-ones were then regioselectively alkylated at N-1 and C-3 to give 1,3,3-trisubstituted indolin-2-ones. The most active series was also prepared by the bis-nitration of m-fluorophenylacetic acid followed by reduction and cyclization to give 6-amino-5-fluoroindolin-2-one. Elaboration to the tetrahydrophthalimide-substituted indolin-2-one was followed by C- and N-alkylation to give the desired compounds.