1801-21-4

Basic information

• Product Name: (2,2-BIINDAN)-1,1,3,3-TETRONE, 2,2-DIPHENYL-
• CAS NO: 1801-21-4
• Molecular Formula: C₃₀H₁₈O₄
• Molecular Weight: 442.471
• Mol File: 1801-21-4.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 663.6°Cat760mmHg
• Flash Point: 299.1°C
• Density: 1.374g/cm³
• CAS DataBase Reference: (2,2-BIINDAN)-1,1,3,3-TETRONE, 2,2-DIPHENYL-(CAS DataBase Reference)
• NIST Chemistry Reference: (2,2-BIINDAN)-1,1,3,3-TETRONE, 2,2-DIPHENYL-(1801-21-4)
• EPA Substance Registry System: (2,2-BIINDAN)-1,1,3,3-TETRONE, 2,2-DIPHENYL-(1801-21-4)

Safety Data

• Hazardous Substances Data: 1801-21-4(Hazardous Substances Data)

Usage

General Description

(2,2-BIINDAN)-1,1,3,3-TETRONE, 2,2-DIPHENYL- is a chemical compound with the molecular formula C26H18O2. It is a tetrone derivative of biphenyl and has a distinct and intricate molecular structure. (2,2-BIINDAN)-1,1,3,3-TETRONE, 2,2-DIPHENYL- is often utilized in the field of organic chemistry for various purposes. Its unique structure and properties make it valuable for research and development in the field of advanced materials and pharmaceuticals. Additionally, it has potential applications in the synthesis of other complex organic compounds. Overall, (2,2-BIINDAN)-1,1,3,3-TETRONE, 2,2-DIPHENYL- is a significant chemical compound with important implications in various scientific and industrial fields.

Upstream product

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

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 articles and documents

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.

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 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