78584-51-7

Basic information

• Product Name: 2-(3-methyl-4-oxopentyl)-1H-isoindole-1,3(2H)-dione
• Synonyms: 2-(3-methyl-4-oxopentyl)-1H-isoindole-1,3(2H)-dione
• CAS NO: 78584-51-7
• Molecular Formula: C₁₄H₁₅NO₃
• Molecular Weight: 245.2738
• Mol File: 78584-51-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(3-methyl-4-oxopentyl)-1H-isoindole-1,3(2H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-methyl-4-oxopentyl)-1H-isoindole-1,3(2H)-dione(78584-51-7)
• EPA Substance Registry System: 2-(3-methyl-4-oxopentyl)-1H-isoindole-1,3(2H)-dione(78584-51-7)

Safety Data

• Hazardous Substances Data: 78584-51-7(Hazardous Substances Data)

Upstream product

• 1074-82-4 potassium phtalimide 
• 1187-81-1 5-chloro-3-methylpentane-2-one 
• 19194-55-9 O-ethyl S-phthalimidomethyl dithiocarbonate 
• 1425508-92-4 2,3,4-trimethyl-4-phenylpent-1-en-3-ol 
• 1123-19-9 3-acetyl-3-methyl-dihydro-furan-2-one 
• 517-23-7 3-acetyl-2-oxo-4,5-dihydrofuran 

Downstream Products

• 78584-62-0 cis-3-acetyl-1,3-dimethyl-3-(3,4,5-trimethoxyphenyl)pyrrolidine 
• 78187-35-6 cis-3-isopropenyl-1,3-dimethyl-2-(3,4,5-trimethoxyphenyl)pyrrolidine 
• 78584-64-2 cis-3-(2-hydroxy-2-propyl)-1,3-dimethyl-2-(3,4,5-trimethoxyphenyl)pyrrolidine 
• 78584-59-5 cis-3-acetyl-3-methyl-2-(3,4,5-trimethoxyphenyl)pyrrolidine 
• 78584-56-2 4,4-ethylenedioxy-3-methyl-N-(3,4,5-trimethoxybenzylidene)pentylamine 
• 78584-60-8 cis-2-(p-chlorophenyl)-3-(1,1-ethylenedioxyethyl)-1,3-dimethylpyrrolidine 
• 78584-66-4 cis-2-(p-chlorophenyl)-3-(1,1-ethylenedioxyethyl)-3-methylpyrrolidine 
• 78584-61-9 cis-3-acetyl-2-(p-chlorophenyl)-1,3-dimethylpyrrolidine 
• 78187-36-7 cis-2-(p-chlorophenyl)-3-isopropenyl-1,3-dimethylpyrrolidine 
• 78584-63-1 cis-(p-chlorophenyl)-3-(2-hydroxy-2-propyl)-1,3-dimethylpyrrolidine 
• 78597-57-6 4,4-ethylenedioxy-3-methyl-N-(p-chlorobenzylidene)pentylamine 
• 78584-58-4 cis-3-acetyl-2-(p-chlorophenyl)-3-methylpyrrolidine 
• 78584-53-9 2,3-dimethyl-1-pyrroline 

Relevant articles and documents

From a remarkable manifestation of polar effects in a radical fragmentation to the convergent synthesis of highly functionalized ketones

A new radical addition/C-C bond fragmentation process is reported. Vinyl carbinols derived from 2-methyl-2-phenylpropanal react with radicals generated from xanthates to give the corresponding ketones. The radical cleavage reaction proceeds under mild conditions, in good to high yield, and in the presence of the unprotected carbinol. Highly functionalized 1,5-diketones and pyridines are readily available using this approach.