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1,3,5-tris(pyridin-4-ylethynyl)benzene is a benzene derivative with the molecular formula C24H15N3, characterized by the presence of three pyridine rings, each featuring an ethynyl group at the 4-position. 1,3,5-tris(pyridin-4-ylethynyl)benzene is distinguished by its unique molecular structure, which contributes to its electrical conductivity and potential applications in electronic devices. Its aromatic nature and rigid backbone also make it a valuable building block in the synthesis of other organic compounds with tailored properties and functionalities.

168289-78-9

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168289-78-9 Usage

Uses

Used in Organic Chemistry:
1,3,5-tris(pyridin-4-ylethynyl)benzene is used as a building block for synthesizing other organic compounds with specific properties and functionalities, owing to its rigid backbone and aromatic nature.
Used in Materials Science:
1,3,5-tris(pyridin-4-ylethynyl)benzene is used as a conductive material in electronic devices due to its ability to conduct electricity, making it a promising candidate for applications in the development of advanced materials for electronics.
Used in Research:
1,3,5-tris(pyridin-4-ylethynyl)benzene is used as a subject of interest for researchers studying molecular architecture and its impact on chemical and physical properties, given its unique molecular structure and potential implications for the design of new materials and compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 168289-78-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,2,8 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 168289-78:
(8*1)+(7*6)+(6*8)+(5*2)+(4*8)+(3*9)+(2*7)+(1*8)=189
189 % 10 = 9
So 168289-78-9 is a valid CAS Registry Number.

168289-78-9SDS

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 1,3,5-tris(2'-ethynyl-4''-pyridyl)benzene

1.2 Other means of identification

Product number -
Other names 4,4',4''-(1,3,5-BENZENETRIYLTRI-2,1-ETHYNEDIYL)TRIS-PYRIDINE

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:168289-78-9 SDS

168289-78-9Downstream Products

168289-78-9Relevant academic research and scientific papers

New coordination polymer networks based on copper(II) hexafluoroacetylacetonate and pyridine containing building blocks: Synthesis and structural study

Winter, Silke,Weber, Edwin,Eriksson, Lars,Csoeregh, Ingeborg

, p. 1808 - 1819 (2006)

The interaction between copper(ii) hexafluoroacetylacetonate [Cu(hfacac)2] and pyridine-containing building blocks with linear, angled and trigonal geometry (1-3) has led to isolation of different coordination polymers (A-D). These were studied

The structures of MOFs prepared from 1,3,5-tris [4-pyridylethynyl]-benzene and a copper(I) perchlorate complex

Yang, En-Che,Wu, Chen-Ming,Pan, Pei-Jia,Lee, Gene-Hsiang,Sheu, Hwo-Shuenn,Chang, Chung-Kai

, p. 1019 - 1026 (2019)

Two copper(I)-based frameworks of complexes {[Cu(L)2(ClO4)]?CH3CN}(2) and {[Cu(L)(ClO4)]? 2CH3CN} (3) (L = 1,3,5-tris(4-pyridylethynyl) benzene) were produced by reacting [Cu(MeCN)4(ClOsub

Modular syntheses of star-shaped pyridine, bipyridine, and terpyridine derivatives by employing sonogashira reactions

Trawny, Daniel,Kunz, Valentin,Reissig, Hans-Ulrich

, p. 6295 - 6302 (2015/03/30)

A simple and flexible synthesis for a series of star-shaped pyridine, bipyridine, and terpyridine derivatives is reported by using a modular approach that combines the use of a ligand, spacer, and core unit. A fairly efficient method to prepare 4′-nonafloxy-functionalized terpyridine derivatives is described. The building blocks that contain the functionalized pyridine, bipyridine, or terpyridine derivatives were linked to different C3-symmetrical core units. In most cases, Sonogashira reactions were employed in the crucial final steps of the synthesis. A star-shaped dodecafluorinated compound was also prepared in a straightforward fashion. A simple procedure for the preparation of partially silylated 1,3,5-triethynylbenzene derivatives is presented, which provides an approach to C2-symmetrical star-shaped compounds that have only one terpyridine and two terphenyl units as "dummy" ligands. The absorption and emission spectra of the fully conjugated C3-symmetrical pyridine derivatives were systematically investigated, and fairly large Stokes shifts were observed.

1,3,5-Tris(functionalised-phenylethynyl)benzene-metal complexes: Synthetic survey of mesoporous coordination polymers and investigation of their carbonisation

Kobayashi, Norifumi,Kijima, Masashi

supporting information; experimental part, p. 1037 - 1045 (2009/05/08)

A series of multicoordinate 1,3,5-tris(functionalised-phenylethynyl) benzenes (1-9) was synthesised, and coordination polymers were constructed from these organic linkers and copper ions in high yields. The carbonisation of the linkers 1-9 afforded a micr

Supramolecular porphyrinic prisms: Coordinative assembly and solution phase X-ray structural characterization

Lee, Suk Joong,Mulfort, Karen L.,O'Donnell, Jodi L.,Zuo, Xiaobing,Goshe, Andrew J.,Wesson, Paul J.,Nguyen, SonBinh T.,Hupp, Joseph T.,Tiede, David M.

, p. 4581 - 4583 (2007/10/03)

Supramolecular porphyrin prisms have been obtained via coordinative self-assembly and characterized by 1H NMR, PFG NMR, electronic absorption spectroscopy and synchrotron-based measurements of solution phase X-ray scattering and diffraction. Th

Octatetrayne-linked porphyrins: "stretched" cyclis dimers and trimers with very spacious cavities

Anderson, Harry L.,Walter, Christopher J.,Vidal-Ferran, Anton,Hay, Robert A.,Lowden, Philip A.,Sanders, Jeremy K. M.

, p. 2275 - 2280 (2007/10/02)

Synthesis are described for two octatetrayne-linked cyclic porphyrin oligomers with extremely spacious cavities.These hosts bind strongly to complementary multidentate guests.Thus, the octatetrayne-linked dimer binds bifunctional ligand bis(4-pyridyl)ethy

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