61599-79-9

Usage

Uses

Used in Organic Synthesis:
Ethanone, 1-(6-iodo-1,3-benzodioxol-5-yl)is used as a building block in organic synthesis for the creation of various biologically active molecules. Its unique structure allows for the development of new compounds with potential applications in different fields.
Used in Pharmaceutical Research:
In pharmaceutical research, Ethanone, 1-(6-iodo-1,3-benzodioxol-5-yl)is utilized as a key component in the preparation of pharmaceutical products. Its properties make it a valuable asset in the development of new drugs and therapeutic agents.
Used in the Development of Biologically Active Molecules:
Ethanone, 1-(6-iodo-1,3-benzodioxol-5-yl)is also used in the development of biologically active molecules, which can have significant implications in medicine and healthcare. Its potential pharmacological properties and therapeutic applications are currently being explored, making it an important compound in the field of pharmaceuticals.
Used in Safety and Hazard Management:
Due to its potential hazards and toxic effects, Ethanone, 1-(6-iodo-1,3-benzodioxol-5-yl)is also used as a reference in safety and hazard management protocols. Understanding its properties and risks can help in the development of proper handling and storage procedures to ensure the safety of researchers and workers in the industry.

InChI:InChI=1/C9H7IO3/c1-5(11)6-2-8-9(3-7(6)10)13-4-12-8/h2-3H,4H2,1H3

Upstream product

• 28657-75-2 2-amino-4,5-methylenedioxy-acetophenone 

Downstream Products

• 1610538-78-7 7-phenylnaphtho[2,3-d][1,3]dioxol-5-ol 
• 1225288-95-8 3,5,6-tris(4-chlorophenyl)-1,2,4-tris(trifluoromethyl)benzene 
• 1620284-96-9 1-(6-((trifluoromethyl)thio)benzo[d][1,3]dioxol-5-yl)ethanone 
• 73252-62-7 2-acetyl-4,5-methylenedioxy-4',5',6'-trimethoxy-1,1'-biphenyl-2-carboxaldehyde anti-O-methyl oxime 

Relevant academic research and scientific papers

A Serendipitous One-Pot Cyanation/Hydrolysis/Enamide Formation: Direct Access to 3-Methyleneisoindolin-1-ones

A direct, one-pot conversion of 2’-haloacetophenones to 3-methyleneisoindolin-1-one scaffolds using CuCN as the sole reagent without the need for moisture-free or anaerobic conditions is reported. This serendipitously discovered transformation with a broa

Palladium Nanoparticles-Catalyzed Synthesis of Indanone Derivatives via Intramolecular Reductive Heck Reaction

An efficient protocol for the straightforward, single-step synthesis of 3-aryl-1-indanones from 2′-iodochalcone via reductive Heck reaction using phosphine free, stable and reusable binaphthyl stabilized palladium nanoparticle (Pd-BNP) as a catalyst has been described. An immense array of substrate scope with electron-rich and deficient 2′-iodochalcones have been synthesized. Further derivatization of product indanones have been achieved successfully. The heterogeneous nature of the Pd-BNP has been validated by centrifugation test and mercury poisoning experiment. Pd-BNP has been successfully recycled up to 5 cycles without any significant loss in reaction yield and particle size of nanoparticles, confirmed by TEM analysis. (Figure presented.).

Copper-Catalyzed Domino Synthesis of 2-Arylthiochromanones through Concomitant C-S Bond Formations Using Xanthate as Sulfur Source

An efficient domino process for the synthesis of thioflavanones has been described using a copper catalyst without addition of any external ligand. A variety of thioflavanones have been synthesized from easily accessible 2′-iodochalcones or 2′-bromochalco

Concise synthesis of 1-naphthols under mild conditions through a copper-catalyzed arylation of methyl ketones

A concise synthesis of 1-naphthols via cyclization of o-iodoacetophenones and methyl ketones has been realized under very mild conditions. The cyclization process is initiated by a rare coppercatalyzed arylation of simple methyl ketones with ortho-iodoacetophenones.

Pd-catalyzed tandem homocoupling-aldol-dehydration of ortho-acylphenyl iodides

A Pd-catalyzed cascade Ullmann coupling-aldol-dehydration reaction of ortho-acylphenyl iodides has been explored. This transformation provides a concise access to colchino analogues in moderate to good yields with wide functional group tolerance.