882-35-9

Basic information

• Product Name: 1-(2-pyridin-1-ylethyl)pyridine dibromide
• Synonyms: 1-(2-pyridin-1-ylethyl)pyridine dibromide;1,1'-Ethylenebis(pyridinium)·dibromide;1,1'-Ethylenebispyridinium·2bromide;1,1'-Ethylenebispyridinium·dibromide
• CAS NO: 882-35-9
• Molecular Formula: 2Br*C₁₂H₁₄N₂
• Molecular Weight: 346.10
• Mol File: 882-35-9.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 313.5°C at 760 mmHg
• Flash Point: 134.8°C
• Appearance: /
• Density: 0.985g/cm³
• Vapor Pressure: 0.000495mmHg at 25°C
• Refractive Index: 1.524
• CAS DataBase Reference: 1-(2-pyridin-1-ylethyl)pyridine dibromide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-pyridin-1-ylethyl)pyridine dibromide(882-35-9)
• EPA Substance Registry System: 1-(2-pyridin-1-ylethyl)pyridine dibromide(882-35-9)

Safety Data

• Hazardous Substances Data: 882-35-9(Hazardous Substances Data)

Usage

Description

1-(2-pyridin-1-ylethyl)pyridine dibromide, with the molecular formula C12H12Br2N2, is a chemical compound that is a dibromide salt. It is synthesized through the reaction of 1-(2-pyridin-1-ylethyl)pyridine with hydrobromic acid. 1-(2-pyridin-1-ylethyl)pyridine dibromide is characterized by its potential utility in various scientific and industrial applications, particularly in the realms of organic synthesis, chemical research, and pharmaceutical development.

Uses

Used in Organic Synthesis:
1-(2-pyridin-1-ylethyl)pyridine dibromide is used as a building block in organic synthesis for the preparation of various functionalized pyridine derivatives. Its unique structure allows for the creation of a wide array of chemical compounds with diverse properties and potential applications.
Used in Chemical Research:
In the field of chemical research, 1-(2-pyridin-1-ylethyl)pyridine dibromide serves as an important compound for studying the properties and reactions of pyridine-based molecules. It aids in understanding the fundamental chemistry of these types of compounds and can lead to the discovery of new reactions or mechanisms.
Used in Pharmaceutical Research:
1-(2-pyridin-1-ylethyl)pyridine dibromide is also utilized in pharmaceutical research as a potential drug candidate. Its structure and properties make it a promising starting point for the development of new medications, particularly those targeting specific biological pathways or receptors.
Used in Medicinal Chemistry:
Within the field of medicinal chemistry, 1-(2-pyridin-1-ylethyl)pyridine dibromide is explored for its potential to be modified and optimized to create new therapeutic agents. Its versatility as a chemical building block allows for the design of molecules with specific biological activities, targeting various diseases and conditions.
Used in Chemical Biology:
1-(2-pyridin-1-ylethyl)pyridine dibromide is also a subject of interest in chemical biology, where it may be used to study the interactions between small molecules and biological targets. This can lead to a better understanding of biological processes and the development of new tools for biological research and drug discovery.

InChI:InChI=1/C12H20N2/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1,3-4,7H,2,5-6,8-12H2

Upstream product

• 110-86-1 pyridine 
• 106-93-4 ethylene dibromide 

Downstream Products

• 110328-05-7 cis-6,7,12a,12b-Tetrahydrodipyrido<1,2-a:2',1'-c>pyrazine 
• 23468-87-3 trans-(+/-)-6,7,12a,12b-Tetrahydrodipyrido<1,2-a:2',1'-c>pyrazine 
• 110-86-1 pyridine 
• 19295-34-2 N-vinyl pyridinium cation 

Relevant articles and documents

A Novel Family of Polyiodo-Bromoantimonate(III) Complexes: Cation-Driven Self-Assembly of Photoconductive Metal-Polyhalide Frameworks

In the presence of different cations, reactions of [SbBr6]3? and I2 result in a new family of diverse supramolecular 1D polyiodide-bromoantimonate networks. The coordination number of Sb, as well as geometry of assembling {Ix}n? polyhalide units, can vary, resulting in unprecedented structural types. The nature of I???Br interactions was studied by DFT calculations; estimated energy values are 1.6–6.9 kcal mol?1. Some of the compounds showed strong photoconductivity in thin films, suggesting multiple feasible applications in optoelectronics and solar energy conversion.

Modulation of Reduction Potentials of Bis(pyridinium)alkane Dications through Encapsulation within Cucurbit[7]uril

Supramolecular modulation of reduction potentials of two series of bis(pyridinium)alkane salts is described. Study of the encapsulation of bis(pyridinium)alkane guests within the CB[7] cavity revealed the critical influence of the linker length and the position of the heteroatom on the reduction potentials of encapsulated guests. CB[7] complexation of pyridinium salts induced reduction potential changes ranging between +50 and -430 mV. Noncovalent modulation of the electron-accepting ability of organic cations can be utilized in electron-transfer-initiated reactions.

Hybrid salts of binuclear Bi(III) halide complexes with 1,2-bis(pyridinium)ethane cation: Synthesis, structure and luminescent behavior

Reactions between 1,2-bis(pyridinium)ethane bromide ((BPE)Br2) and [BiCl6]3-/[BiBr6]3- in HCl or HBr results in isostructural binuclear complexes (BPE)2[Bi2X10] (X = Cl (1) and Br (2)) which were characterized by X-ray diffractometry, IR and Raman spectroscopy. Both complexes manifest orange-red luminescence in solid state.

Bromoantimonates with bis(pyridinium)-type dications obtained via oxidation by dibromine: Diverse structural types and features of interactions pattern

Bromoantimonate(III) species, which can be generated in solution by reaction of Sb2O3 and HBr, can be oxidized by Br2 into mixed-valence complexes or bromoantimonates(V). The outcome of these reactions governs by the nature of cation which salt is used for isolation of solid complexes. Using bromides of three 1,n-bis(pyridinium)alkane cations (PyCn, where X = 2, 3 and 4), we isolated three complexes: (PyC2){[SbBr6](Br3)} (1), (PyC3)2[Sb2Br9][SbBr6] (2) and (PyC4){[SbBr6](Br3)} (3), respectively. Their structures were determined by X-ray diffractometry. For 1 and 3, the energies of non-covalent interactions between tribromide units and [SbBr6]? were estimated using DFT calculations.