29874-34-8

Usage

Derivative of indane-1,3-dione

The compound is derived from the parent molecule indane-1,3-dione, which means it has a similar structure with some modifications.

Benzo[3,4-d][1,3]dioxole-5-ylmethylene substituent

The compound contains a specific functional group, benzo[3,4-d][1,3]dioxole-5-ylmethylene, which is attached to the indane-1,3-dione core structure.

Unique structural features

The presence of the benzo[3,4-d][1,3]dioxole-5-ylmethylene group gives 2-(BENZO[3,4-D]1,3-DIOXOLEN-5-YLMETHYLENE)INDANE-1,3-DIONE a unique structure, which may contribute to its potential applications.

Potential applications in organic synthesis

Due to its unique structure, the compound may be useful as an intermediate or building block in the synthesis of other organic compounds.

Potential applications in medicinal chemistry

The compound's unique structure may also make it a promising candidate for the development of new pharmaceuticals or therapeutic agents.

Further studies needed

To fully explore the potential uses and properties of 2-(BENZO[3,4-D]1,3-DIOXOLEN-5-YLMETHYLENE)INDANE-1,3-DIONE, additional research and experimentation are required.

Upstream product

• 606-23-5 1H-indene-1,3(2H)-dione 
• 120-57-0 piperonal 
• 3457-77-0 1,3-dioxo-indan-2-carboxylic acid ethyl ester 
• 27738-39-2 piperonal-phenylimine 

Relevant academic research and scientific papers

Leishmanicidal and cytotoxic activities and 4D-QSAR of 2-arylidene indan-1,3-diones

The indan-1,3-dione and its derivatives are important building blocks in organic synthesis and present important biological activities. Herein, the leishmanicidal and cytotoxicity evaluation of 16 2-arylidene indan-1,3-diones is described. The compounds w

Zirconium catalyzed synthesis of 2-arylidene Indan-1,3-diones and evaluation of their inhibitory activity against NS2B-NS3 WNV protease

A simple and efficient Knoevenagel procedure for the synthesis of 2-arylidene indan-1,3-diones is herein reported. These compounds were prepared via ZrOCl2·8H2O catalyzed reactions of indan-1,3-dione with several aromatic aldehydes and using water as the

The First Organocatalytic Hetero-Domino Knoevenagel-Diels-Alder-Epimerization Reactions: Diastereoselective Synthesis of Highly Substituted Spiro[cyclohexane-1,2′-indan]-1′,3′ ,4-triones

L-Proline and pyrrolidine catalyzed the three component hetero-domino Knoevenagel-Diels-Alder-Epimerization reactions of readily available precursors enones 1a-i, arylaldehydes 2a-i and 1,3-indandione 3 to furnish highly substituted prochiral spiro[cycloh

Behaviour of 2-substituted 1,3-indandiones towards aldimines

Treatment of 2-cyano-1,3-indandione (1) with aldimines gave the expected Mannich bases (2-4), while the arylidenes (7,8) were obtained when 2-ethoxyearbonyl-1,3-indandione (5) was subjected to react with aldimines. On the other hand, treatment of 2-acetyl

A study on the reaction of 1,3-indandione with Schiff bases: Synthesis of new 1,3-indandiones with expected psychopharmacological and anticoagulant activity

Condensation of the title compound 1 with aldimines gave the 2-arylidene derivatives 3-9 instead of the expected Mannich bases 2. Compounds 10-11 were obtained from 1 and aldimines of α-ketoaldehydes. Isatin-anil (12) reacts with 1 to give 13. However, th

Anionic Activation of Organic Compounds by Adsorption on Alumina and Alumina-KF

Condensations of acidic carbon compounds with piperonal (1) were achieved by adsorption on neutral alumina without solvent for the more acidic compounds and on Al2O3-KF for the less acidic compounds; dry Michael condensations also took place on Al2O3-KF.