112476-34-3

Usage

Structure

1H-Isoindol-1-one, 2,3,3a,6,7,7a-hexahydro-2-(phenylmethyl)-, cis-

Appearance

White to off-white powder

Molecular weight

231.3 g/mol

Isomerism

cis-isomer of 1H-isoindol-1-one

Uses

Organic synthesis, pharmaceutical research (potential pharmacological effects and applications in medicine and other industries may warrant further investigation)

Upstream product

• 112476-33-2 N-Benzyl-N-((E)-penta-2,4-dienyl)-acrylamide 
• 112476-33-2 N-Benzyl-N-((E)-penta-2,4-dienyl)-acrylamide 
• 814-68-6 acryloyl chloride 
• 52022-82-9 (E)-5-bromopenta-1,3-diene 
• 115477-07-1 (E)-N-benzylpenta-2,4-dien-1-amine 
• 100-46-9 benzylamine 

Relevant academic research and scientific papers

Synthesis of Hydroisoindoles via Intramolecular Diels-Alder Reactions of Functionalised Amido Trienes

Reactions of amino dienes with acryloyl chloride, maleic anhydride, bromomaleic anhydride, and dichloromaleic anhydride were studied.Acylation and intramolecular reaction by Diels-Alder cyclisation gave bicyclic adducts.Adducts of dichloromaleic anhydride

New features of the intramolecular Diels Alder route to hydroisoindoles

Regio- and stereo- controlled routes to functionalised hydroisoindoles have been developed by reaction of aminodienes with unsaturated anhydrides or acid chlorides and subsequent elaboration of the Diels Alder adducts.