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(2-CHLORO-PHENYL)-(2,3,4,5-TETRAPHENYL-CYCLOPENTA-2,4-DIENYLIDENE)-AMINE is a complex amine compound characterized by the presence of a chloro-phenyl group and a tetraphenyl-cyclopenta-2,4-dienylidene group. As a derivative of ammonia, it features a nitrogen atom bonded to alkyl or aryl groups, which may confer unique chemical properties and potential applications in fields such as pharmaceuticals, materials science, or organic synthesis.

869668-10-0

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  • (2-CHLORO-PHENYL)-(2,3,4,5-TETRAPHENYL-CYCLOPENTA-2,4-DIENYLIDENE)-AMINE

    Cas No: 869668-10-0

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869668-10-0 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.

Check Digit Verification of cas no

The CAS Registry Mumber 869668-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,6,6 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 869668-10:
(8*8)+(7*6)+(6*9)+(5*6)+(4*6)+(3*8)+(2*1)+(1*0)=240
240 % 10 = 0
So 869668-10-0 is a valid CAS Registry Number.

869668-10-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-chlorophenyl)-2,3,4,5-tetraphenylcyclopenta-2,4-dien-1-imine

1.2 Other means of identification

Product number -
Other names 2-CHLORO-N-(2,3,4,5-TETRAPHENYLCYCLOPENTA-2,4-DIENYLIDENE)ANILINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:869668-10-0 SDS

869668-10-0Downstream Products

869668-10-0Relevant 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

Hu, Qiaoshu,Lu, Jiang,Wang, Congyang,Wang, Chao,Xi, Zhenfeng

, p. 6614 - 6624 (2008/02/05)

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

Lu, Jiang,Mao, Guoliang,Zhang, Wenxiong,Xi, Zhenfeng

, p. 4848 - 4850 (2007/10/03)

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.

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