26487-02-5

Basic information

• Product Name: 3-ethoxy-1-isoindolinone
• Synonyms: 3-ethoxy-1-isoindolinone
• CAS NO: 26487-02-5
• Molecular Formula: C₁₀H₁₁NO₂
• Molecular Weight: 177.19984
• Mol File: 26487-02-5.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-ethoxy-1-isoindolinone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-ethoxy-1-isoindolinone(26487-02-5)
• EPA Substance Registry System: 3-ethoxy-1-isoindolinone(26487-02-5)

Safety Data

• Hazardous Substances Data: 26487-02-5(Hazardous Substances Data)

Upstream product

• 136918-14-4 phthalimide 
• 64-17-5 ethanol 
• 26486-93-1 3-hydroxy-2,3-dihydro-isoindol-1-one 
• 7468-67-9 o-formylbenzonitrile 
• 7647-01-0 hydrogenchloride 
• 7732-18-5 water 
• 1062261-30-6 ethyl 2-(azidomethyl)benzoate 

Downstream Products

• 26486-93-1 3-hydroxy-2,3-dihydro-isoindol-1-one 
• 123783-84-6 3-((Z)-3-Phenyl-allyloxy)-2,3-dihydro-isoindol-1-one 
• 123783-93-7 (S)-3-((R)-1-Benzyl-allyloxy)-2,3-dihydro-isoindol-1-one 
• 123783-93-7 (S)-3-((S)-1-Benzyl-allyloxy)-2,3-dihydro-isoindol-1-one 
• 123783-92-6 (S)-3-((R)-1-Phenethyl-allyloxy)-2,3-dihydro-isoindol-1-one 
• 123783-92-6 (S)-3-((S)-1-Phenethyl-allyloxy)-2,3-dihydro-isoindol-1-one 
• 98289-81-7 (3R,9bR)-3-Ethyl-2,3-dihydro-9bH-oxazolo[2,3-a]isoindol-5-one 
• 98289-81-7 (3S,9bR)-3-Ethyl-2,3-dihydro-9bH-oxazolo[2,3-a]isoindol-5-one 
• 123783-85-7 3-((E)-3-Phenyl-allyloxy)-2,3-dihydro-isoindol-1-one 
• 123783-99-3 (2R,3R,9bR)-2-Benzyl-3-methyl-2,3-dihydro-9bH-oxazolo[2,3-a]isoindol-5-one 
• 123783-99-3 (2R,3S,9bR)-2-Benzyl-3-methyl-2,3-dihydro-9bH-oxazolo[2,3-a]isoindol-5-one 
• 123783-98-2 (2R,3R,9bR)-3-Methyl-2-phenethyl-2,3-dihydro-9bH-oxazolo[2,3-a]isoindol-5-one 
• 123783-98-2 (2R,3S,9bR)-3-Methyl-2-phenethyl-2,3-dihydro-9bH-oxazolo[2,3-a]isoindol-5-one 
• 93679-80-2 3-p-toluidino-isoindolin-1-one 

Relevant articles and documents

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A REMOVABLE AUXILIARY FOR AMIDOMERCURATION REACTIONS: THE STEREOCONTROLLED PREPARATION OF VICINAL AMINOALCOHOLS

Unsaturated amidals 1, derived from allylic alcohols and containing a stereogenic amidal center, undergo amidomercuration with high 1,3-stereoinduction from the amidal center.In substrates derived from secondary allylic alcohols, the influence of the ster

Reduction of O alkylated imides

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