869668-10-0

Basic information

• Product Name: (2-CHLORO-PHENYL)-(2,3,4,5-TETRAPHENYL-CYCLOPENTA-2,4-DIENYLIDENE)-AMINE
• Synonyms: (2-CHLORO-PHENYL)-(2,3,4,5-TETRAPHENYL-CYCLOPENTA-2,4-DIENYLIDENE)-AMINE
• CAS NO: 869668-10-0
• Molecular Formula: C35H24ClN
• Molecular Weight: 494.02
• Mol File: 869668-10-0.mol

Chemical Properties

• Melting Point: 189-190 °C
• Boiling Point: 665.0±55.0 °C(Predicted)
• Appearance: /
• Density: 1.12±0.1 g/cm3(Predicted)
• PKA: 2.86±0.60(Predicted)
• CAS DataBase Reference: (2-CHLORO-PHENYL)-(2,3,4,5-TETRAPHENYL-CYCLOPENTA-2,4-DIENYLIDENE)-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: (2-CHLORO-PHENYL)-(2,3,4,5-TETRAPHENYL-CYCLOPENTA-2,4-DIENYLIDENE)-AMINE(869668-10-0)
• EPA Substance Registry System: (2-CHLORO-PHENYL)-(2,3,4,5-TETRAPHENYL-CYCLOPENTA-2,4-DIENYLIDENE)-AMINE(869668-10-0)

Safety Data

• Hazardous Substances Data: 869668-10-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(2-CHLORO-PHENYL)-(2,3,4,5-TETRAPHENYL-CYCLOPENTA-2,4-DIENYLIDENE)-AMINE is used as a pharmaceutical compound for its potential therapeutic effects. The specific molecular structure may allow it to interact with biological targets or be modified for specific medicinal purposes, although further research is needed to explore its full potential in this area.
Used in Materials Science:
In the field of materials science, (2-CHLORO-PHENYL)-(2,3,4,5-TETRAPHENYL-CYCLOPENTA-2,4-DIENYLIDENE)-AMINE may be utilized for the development of new materials with unique properties. Its chemical structure could contribute to the creation of advanced materials with applications in various industries, pending further investigation into its properties and behavior.
Used in Organic Synthesis:
(2-CHLORO-PHENYL)-(2,3,4,5-TETRAPHENYL-CYCLOPENTA-2,4-DIENYLIDENE)-AMINE can be employed as a synthetic building block or intermediate in organic synthesis. Its distinct chemical features may enable the synthesis of novel organic compounds with a range of applications, from specialty chemicals to complex organic molecules.
Further research and analysis are essential to fully understand the characteristics and potential uses of (2-CHLORO-PHENYL)-(2,3,4,5-TETRAPHENYL-CYCLOPENTA-2,4-DIENYLIDENE)-AMINE, as its complex structure suggests a wide range of possible applications that are yet to be discovered and validated.

Upstream product

• 3320-83-0 o-chlorophenyl isocyanate 
• 501-65-5 diphenyl acetylene 

Relevant articles and documents

Lewis acid-controlled reactions of zirconacyclopentadienes with isocyanates and isothiocyanates. One-pot three- or four-component synthesis of multiply substituted iminocyclopentadienes and butadiene-tethered 1,6-bisamides and electrophilic cyclization

Multiply substituted zirconacyclopentadienes including bicyclic zirconacyclopentadienes and zirconaindenes reacted with isocyanates and isothiocyanates in the presence of Lewis acids to afford iminocyclopentadienes and conjugated 1,6-bisamides, depending on the nature of Lewis acids, isocyanates, and isothiocyanates used. Only in the presence of BF3 could iminocyclopentadienes be obtained in high isolated yields when zirconacyclopentadienes were treated with isocyanates. On the contrary, BF3 could not mediate the reaction of zirconacyclopentadienes with isothiocyanates. For the reactions of zirconacyclopentadienes with isothiocyanates, EtAlCl2 was found effective to generate iminocyclopentadienes as the products. Interestingly, however, for the reactions of zirconacyclopentadienes with isocyanates, EtAlCl2 was found to work very differently from BF3. Instead of iminocyclopentadienes, conjugated 1,6-bisamides and conjugated mono-amides were obtained as products in high isolated yields from the reactions of zirconacyclopentadienes with isocyanates, depending on the substituents of isocyanates. The reaction path and products could be controlled by Lewis acids. As a demonstration of the usefulness of thus obtained unsaturated bisamides, electrophilic cyclization using acids, NBS, and I2 was carried out. Electrophilic cyclization of multisubstituted conjugated 1,6-bisamide derivatives afforded cyclic iminoethers in excellent yields with perfect selectivity. Only one of the amide groups took part in the electrophilic cyclization.

Lewis acid-promoted reactions of zirconacyclopentadienes with isocyanates. A one-pot three-component synthesis of multiply-substituted iminocyclopentadienes from one isocyanate and two alkynes

Multiply-substituted iminocyclopentadienes were formed from Lewis acid-promoted reactions of zirconacyclopentadienes and isocyanates via a one-pot three-component coupling process; the C=O double bond of the RN=C=O moiety in the isocyanate was cleaved, and the isocyanates behaved formally as a one-carbon unit with Lewis acid-dependent and substituent-dependent reactions being realized. The Royal Society of Chemistry 2005.