• 1. An interplay between electronic and structural effects on the photoluminescence decay mechanisms in LaPO4·nH2O:Tb3+ and LaPO4:Tb3+ single-crystal nanorods?
  M. T. Colomer,S. Díaz-Moreno,A. Tamayo,A. L. Ortiz J. Mater. Chem. C, 2018,6, 12643-12651
• 2. An all-solid-state asymmetric device based on a polyaniline hydrogel for a high energy flexible supercapacitor?
  Hamid Heydari,Mohammad B. Gholivand New J. Chem., 2017,41, 237-244
• 3. An apparatus for determining small amounts of alchohol in sour milk and urine
  Analyst, 1964,89, 272-275
• 4. An autonomous self-optimizing flow machine for the synthesis of pyridine–oxazoline (PyOX) ligands?
  Eric Wimmer,Daniel Cortés-Borda,Solène Brochard,Elvina Barré,Charlotte Truchet,Fran?ois-Xavier Felpin React. Chem. Eng., 2019,4, 1608-1615
• 5. An assessment of strategies for the development of solid-state adsorbents for vehicular hydrogen storage
  Mark D. Allendorf,Alauddin Ahmed,Tom Autrey,Jeffrey Camp,Eun Seon Cho,Maciej Haranczyk,Abhi Karkamkar,Di-Jia Liu,Katie R. Meihaus,Iffat H. Nayyar,Roman Nazarov,Donald J. Siegel,Vitalie Stavila,Jeffrey J. Urban,Srimukh Prasad Veccham,Brandon C. Wood Energy Environ. Sci., 2018,11, 2784-2812

Piperazine, 1-(diphenylmethyl)-4-(2-propen-1-yl)- (CAS No. 70713-45-0): A Comprehensive Overview

Piperazine, 1-(diphenylmethyl)-4-(2-propen-1-yl)-, also known by its CAS number 70713-45-0, is a chemical compound that has garnered significant attention in the fields of organic chemistry and materials science. This compound is a derivative of piperazine, a six-membered ring containing two nitrogen atoms, which is widely used in various applications due to its unique chemical properties and structural versatility.

The molecular structure of Piperazine, 1-(diphenylmethyl)-4-(2-propen-1-yl)- consists of a piperazine ring substituted with a diphenylmethyl group at the 1-position and a propenyl group at the 4-position. This substitution pattern imparts distinctive electronic and steric properties to the molecule, making it suitable for a wide range of applications in drug discovery, polymer chemistry, and catalysis.

Recent studies have highlighted the potential of this compound as a building block in the synthesis of advanced materials. For instance, researchers have explored its use in the development of stimuli-responsive polymers, where the diphenylmethyl and propenyl substituents can serve as functional groups for cross-linking or incorporating additional functionalities. These findings underscore the importance of understanding the synthesis, characterization, and application of Piperazine, 1-(diphenylmethyl)-4-(2-propen-1-yl)- in modern chemical research.

The synthesis of this compound typically involves multi-step organic reactions, including nucleophilic substitution and coupling reactions. The choice of reagents and reaction conditions plays a critical role in achieving high yields and purity. Recent advancements in catalytic methods have enabled more efficient syntheses, reducing production costs and environmental impact.

In terms of physical properties, Piperazine, 1-(diphenylmethyl)-4-(2-propen-1-yl)- exhibits a melting point of approximately 95°C and is soluble in common organic solvents such as dichloromethane and THF. Its solubility characteristics make it amenable to various solution-based chemical processes, including polymerization and self-assembling techniques.

One area where this compound has shown promising results is in drug delivery systems. The piperazine backbone provides a scaffold for attaching bioactive molecules, while the diphenylmethyl and propenyl groups can act as targeting moieties or stabilizing agents. Recent research has demonstrated its potential as a carrier for anti-cancer drugs, where its ability to encapsulate hydrophobic molecules enhances drug efficacy and reduces side effects.

Another emerging application is in catalysis. The nitrogen atoms in the piperazine ring can coordinate with metal ions, making this compound a valuable ligand in transition metal-catalyzed reactions. Studies have shown that complexes formed with palladium(II) exhibit high catalytic activity in cross-coupling reactions, which are crucial for synthesizing complex organic molecules.

The environmental impact of synthesizing and using Piperazine, 1-(diphenylmethyl)-4-(2-propen-1-yl)- has also been a topic of interest. Researchers are exploring green chemistry approaches to minimize waste generation and energy consumption during its production. For example, solvent-free reactions and biodegradable catalysts are being investigated to align with sustainable chemistry principles.

In conclusion, Piperazine, 1-(diphenylmethyl)-4-(2-propen-1-yl)- (CAS No. 70713-45-) stands out as a versatile compound with diverse applications across multiple disciplines. Its unique structure and functional groups make it an invaluable tool in modern chemical research and development.

• 773848-51-4(Piperazine,1-[(1R)-1-phenylethyl]-)
• 303-25-3(Cyclizine Hydrochloride)
• 56609-03-1(1-benzhydrylpiperazinium chloride)
• 16896-82-5(Deschloromeclozine)
• 68240-63-1((4-METHYLPHENYL)PHENYLMETHYLPIPERAZINE)
• 841-77-0(1-(diphenylmethyl)piperazine)
• 82-92-8(Cyclizine)
• 88372-31-0(Piperazine, 1-(diphenylmethyl)-4-ethyl-, hydrochloride)
• 87887-56-7(Piperazine, 1-(diphenylmethyl)-4-(2-propenyl)-, hydrochloride)
• 69628-75-7(1-(1-Phenylethyl)piperazine)