1801-21-4

Usage

Uses

Used in Organic Chemistry Research:
(2,2-BIINDAN)-1,1,3,3-TETRONE, 2,2-DIPHENYLis used as a research compound for studying its unique structure and properties. Its distinct molecular arrangement makes it a valuable subject for investigations in organic chemistry.
Used in Advanced Materials Development:
In the field of advanced materials, (2,2-BIINDAN)-1,1,3,3-TETRONE, 2,2-DIPHENYLis used as a component in the development of new materials with specific properties. Its unique characteristics contribute to the creation of innovative materials with potential applications in various industries.
Used in Pharmaceutical Research and Development:
(2,2-BIINDAN)-1,1,3,3-TETRONE, 2,2-DIPHENYLis utilized as a starting material or intermediate in the synthesis of pharmaceutical compounds. Its potential role in drug development makes it an important compound in the pharmaceutical industry.
Used in Synthesis of Complex Organic Compounds:
(2,2-BIINDAN)-1,1,3,3-TETRONE, 2,2-DIPHENYLis used as a reactant in the synthesis of other complex organic compounds. Its ability to participate in various chemical reactions makes it a useful building block in organic synthesis.

Upstream product

• 64-17-5 ethanol 
• 6156-43-0 2-phenyl-indan-1,3-dione; sodium-salt 
• 100-52-7 benzaldehyde 
• 87-41-2 2-benzofuran-1(3H)-one 
• 83-12-5 phenindione 
• 110-46-3 isopentyl nitrite 
• 1801-20-3 2-bromo-2-phenyl-indan-1,3-dione 

Downstream Products

• 22253-13-0 1-Phenyl-2-(1-phenyl-inden-2)-indan 
• 96970-09-1 2,2'-Diphenyl-2,2'-biindan-1,1',3,3'-tetrol 
• 1801-22-5 1-(1,3-Dioxo-hydrindyl-⁽²⁾)-2-(1,3-dioxo-2-phenyl-hydrindyl-⁽²⁾)-benzol 
• 4505-48-0 2-phenylindene 

Relevant academic research and scientific papers

A facile copper(i)-catalyzed homo-coupling of indanone derivatives using diaziridinone under mild conditions

A novel and efficient Cu(i)-catalyzed homo-coupling of indanone derivatives using diaziridinone as an oxidant is described. A variety of 1,4-dicarbonyl compounds bearing two adjacent quaternary stereocenters were obtained in high yields with high diastereoselectivities via a base-free and operationally simple process under mild reaction conditions.

A dinuclear palladium catalyst for α-Hydroxylation of carbonyls with O2

A chemo- and regioselective α-hydroxylation reaction of carbonyl compounds with molecular oxygen as oxidant is reported. The hydroxylation reaction is catalyzed by a dinuclear Pd(II) complex, which functions as an oxygen transfer catalyst, reminiscent of an oxygenase. The development of this oxidation reaction was inspired by discovery and mechanism evaluation of previously unknown Pd(III)-Pd(III) complexes.

Pd/C-catalyzed direct α-oxygenation of 1,3-dicarbonyl compounds using molecular oxygen

A hydroxyl group was readily and directly introduced into the α-position of a variety of β-dicarbonyl compounds by heterogeneous Pd/C-catalyzed oxygenation using molecular oxygen. Georg Thieme Verlag Stuttgart.

Synthesis and pharmacological properties of sulfur derivatives of indane-1,3-dione

Synthesis of sulfur derivatives of indane-1,3-dione, VIIb-c, VIIIa-b, IX and X is described. Results of a preliminary pharmacological screening of six compounds [VIIb, VIII, VIIIb, IX, X and XI] are presented.

Synthesis of Fused Benzofuranes by Dehydratation of Cyclic Phenyl-β-dicarbonyl Compounds

3-Hydroxy-3-phenyl-quinoline-2,4-diones (1) cyclize on treatment with strong acids to give benzofuroquinolones (3).In analogy, 2-hydroxy-2-phenylphenalenedione (7) furnishes the benzofurophenalenone 10. - Keywords: Benzofuranes; Phenyl-β-dicarbonyl compou