913819-57-5

Basic information

• Product Name: 5-hydroxy-4-isopropyl-1-(2-isopropyl-6-methyl-phenyl)-5-methyl-2-oxo-2,5-dihydro-1H-pyrrole-3-carbonitrile
• Synonyms: 5-hydroxy-4-isopropyl-1-(2-isopropyl-6-methyl-phenyl)-5-methyl-2-oxo-2,5-dihydro-1H-pyrrole-3-carbonitrile
• CAS NO: 913819-57-5
• Molecular Weight: 312.412
• Mol File: 913819-57-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-hydroxy-4-isopropyl-1-(2-isopropyl-6-methyl-phenyl)-5-methyl-2-oxo-2,5-dihydro-1H-pyrrole-3-carbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 5-hydroxy-4-isopropyl-1-(2-isopropyl-6-methyl-phenyl)-5-methyl-2-oxo-2,5-dihydro-1H-pyrrole-3-carbonitrile(913819-57-5)
• EPA Substance Registry System: 5-hydroxy-4-isopropyl-1-(2-isopropyl-6-methyl-phenyl)-5-methyl-2-oxo-2,5-dihydro-1H-pyrrole-3-carbonitrile(913819-57-5)

Safety Data

• Hazardous Substances Data: 913819-57-5(Hazardous Substances Data)

Upstream product

• 545372-75-6 2-cyano-N-(2-isopropyl-6-methylphenyl)acetamide 
• 7493-58-5 4-methyl-2,3-pentanedione 
• 5266-85-3 2-isopropyl-6-methylaniline 

Relevant articles and documents

LIGANDS FOR THE MODULATION OF ECDYSONE RECEPTORS AND CONTROL OF INSECT GROWTH

The present invention relates to the use of N-substituted γ-methylene γ-lactams as non-steroidal ligands for modulating ecdysone receptors generally and, in particular, ecdysone receptors of the Australian blowfly, Lucilia cuprina. The present invention f

Synthesis of N-substituted γ-methylene γ-lactams

N-Substituted cyanoacetamides 1 were condensed with 1,2-diketones 2 under base catalysis to form ?-hydroxy ?-lactams 3. Treatment of 3 with acids gave novel fungicidal ?-methylene ?-lactams 4. The exocyclic double bond of 4b reacted reversibly with 4-toluene sulfinate. CSIRO 2005.