1945-84-2,MFCD00041598
Catalog No.:AA003H5J

1945-84-2 | 2-Ethynylpyridine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
>97%
in stock  
$16.00   $11.00
- +
5g
>97%
in stock  
$41.00   $29.00
- +
10g
>97%
in stock  
$68.00   $48.00
- +
100g
98%
in stock  
$662.00 $464.00
  • Technical Information
  • Properties
  • Literature
  • Application
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003H5J
Chemical Name:
2-Ethynylpyridine
CAS Number:
1945-84-2
Molecular Formula:
C7H5N
Molecular Weight:
103.1213
MDL Number:
MFCD00041598
SMILES:
C#Cc1ccccn1
Properties
Properties
 
BP:
170.5°C at 760 mmHg  
Form:
Liquid  
MP:
77-78 C  
Refractive Index:
n20/D 1.56(lit.)  
Storage:
Inert atmosphere;-20 ℃;  

Computed Properties
 
Complexity:
109  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1  

Synonyms
 
945E842  
Literature

Title: Nickel complexes with 'click'-derived pyridyl-triazole ligands: weak intermolecular interactions and catalytic ethylene oligomerisation.

Journal: Dalton transactions (Cambridge, England : 2003) 20121107

Title: Formation of higher-order structures of chiral poly(ethynylpyridine)s depending on size, temperature, and saccharide recognition.

Journal: Organic & biomolecular chemistry 20120914

Title: Concentration- and time-dependent eccentric changes in circular dichroism of saccharide-linked ethynylpyridine oligomer with copper(II) ions.

Journal: The Journal of organic chemistry 20120601

Title: Synthesis and properties of a water-soluble ionic conjugated polymer with carboxylic acids.

Journal: Journal of nanoscience and nanotechnology 20120501

Title: Copper(II)/phenanthroline-mediated CD-enhancement and chiral memory effect on a meta-ethynylpyridine oligomer.

Journal: Chemical communications (Cambridge, England) 20120404

Title: Synthesis, structural charaterization, and electrochemical and optical properties of ferrocene-triazole-pyridine triads.

Journal: Inorganic chemistry 20110905

Title: Synthesis and characterization of a polyacetylene derivative with phenylazobenzene moieties.

Journal: Journal of nanoscience and nanotechnology 20110801

Title: Copper(II)-mediated chiral helicity amplification and inversion of meta-ethynylpyridine polymers with metal coordination sites.

Journal: Chemical communications (Cambridge, England) 20110714

Title: Potent mGluR5 antagonists: pyridyl and thiazolyl-ethynyl-3,5-disubstituted-phenyl series.

Journal: Bioorganic & medicinal chemistry letters 20110601

Title: Hydrogen bond partner reorganization in the coadsorption of a monodendron and pyridylethynyl derivatives.

Journal: Langmuir : the ACS journal of surfaces and colloids 20110215

Title: Preparation of ethynylpyridine macrocycles by oxidative coupling of an ethynylpyridine trimer with terminal acetylenes.

Journal: The Journal of organic chemistry 20110107

Title: Engineering of linear molecular nanostructures by a hydrogen-bond-mediated modular and flexible host-guest assembly.

Journal: ACS nano 20101026

Title: Removal and leakage of environmental tobacco smoke from a model smoking room.

Journal: Journal of occupational and environmental hygiene 20101001

Title: Ligand-assisted J-type aggregates of zinc porphyrin: anticooperative molecular organization in self-assembled bolaamphiphile.

Journal: Organic & biomolecular chemistry 20100807

Title: Cyclometallated platinum(II) complexes containing pyridyl-acetylide ligands: the selective influence of lead binding on luminescence.

Journal: Dalton transactions (Cambridge, England : 2003) 20100121

Title: New 1,2,3-triazole ligands through click reactions and their palladium and platinum complexes.

Journal: Dalton transactions (Cambridge, England : 2003) 20091114

Title: 2-[1-(1-Naphth-yl)-1H-1,2,3-triazol-4-yl]pyridine.

Journal: Acta crystallographica. Section E, Structure reports online 20090501

Title: 1-(3-Bromo-prop-yl)-4-(2-pyrid-yl)-1H-1,2,3-triazole.

Journal: Acta crystallographica. Section E, Structure reports online 20090501

Title: Control of the photoreactivity of diarylethene derivatives by quaternarization of the pyridylethynyl group.

Journal: Organic letters 20080515

Title: A new series of dinuclear Au(I) complexes linked by diethynylpyridine groups.

Journal: Dalton transactions (Cambridge, England : 2003) 20080328

Title: Helix formation in synthetic polymers by hydrogen bonding with native saccharides in protic media.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20061016

Title: Regulation of saccharide binding with basic poly(ethynylpyridine)s by H+-induced helix formation.

Journal: Journal of the American Chemical Society 20051123

Application
2-Ethynylpyridine is a chemical compound commonly employed as a versatile building block in organic synthesis. Its molecular structure consists of a pyridine ring with an ethynyl group (-C≡CH) attached to the 2-position, making it highly reactive and suitable for various reactions leading to the formation of diverse organic compounds.

One significant application of 2-ethynylpyridine is in the synthesis of conjugated polymers. Through polymerization reactions, 2-ethynylpyridine can be polymerized to form polymers with unique properties. For example, it can be polymerized to yield poly(2-ethynyl-N-iodopyridinium iodide), poly[2-ethynyl-N-(2-furoyl)pyridinium chloride, and poly[2-ethynyl-N-(propylsulfonate)pyridinium betaine]. These polymers exhibit different functionalities and can find applications in areas such as optoelectronics, materials science, and biomedical engineering.

Additionally, 2-ethynylpyridine can react with various reagents to produce functionalized derivatives. For instance, its reaction with anionic heptaphosphide clusters yields the 4-(2′-pyridyl)-1,2,3-triphospholide anion, which may have applications in coordination chemistry and catalysis.

Moreover, 2-ethynylpyridine can be incorporated into water-soluble ionic conjugated polymers, such as poly[N-(carboxymethyl)-2-ethynylpyridinium bromide], enabling their use in aqueous environments for applications in sensors, drug delivery, and biomedical research.

Furthermore, 2-ethynylpyridine can undergo self-doping reactions to form self-doped ionic conjugated polymers like poly(2-ethynylpyridinimum N-benzoylsulfonate), which possess enhanced conductivity and stability, making them suitable for electronic and optoelectronic applications.

In summary, 2-ethynylpyridine serves as a valuable building block in organic synthesis, enabling the preparation of conjugated polymers and functionalized derivatives with diverse properties and potential applications in various fields of science and technology.
Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Related Products of 1945-84-2
Tags:1945-84-2 Molecular Formula|1945-84-2 MDL|1945-84-2 SMILES|1945-84-2 2-Ethynylpyridine
Catalog No.: AA003H5J
1945-84-2,MFCD00041598
1945-84-2 | 2-Ethynylpyridine
Pack Size: 1g
Purity: >97%
in stock
$16.00 $11.00
Pack Size: 5g
Purity: >97%
in stock
$41.00 $29.00
Pack Size: 10g
Purity: >97%
in stock
$68.00 $48.00
Pack Size: 100g
Purity: 98%
in stock
$662.00 $464.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003H5J
Chemical Name: 2-Ethynylpyridine
CAS Number: 1945-84-2
Molecular Formula: C7H5N
Molecular Weight: 103.1213
MDL Number: MFCD00041598
SMILES: C#Cc1ccccn1
Properties
BP: 170.5°C at 760 mmHg  
Form: Liquid  
MP: 77-78 C  
Refractive Index: n20/D 1.56(lit.)  
Storage: Inert atmosphere;-20 ℃;  
Complexity: 109  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 8  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1  
60: 945E842  
Literature fold

Title: Nickel complexes with 'click'-derived pyridyl-triazole ligands: weak intermolecular interactions and catalytic ethylene oligomerisation.

Journal: Dalton transactions (Cambridge, England : 2003)20121107

Title: Formation of higher-order structures of chiral poly(ethynylpyridine)s depending on size, temperature, and saccharide recognition.

Journal: Organic & biomolecular chemistry20120914

Title: Concentration- and time-dependent eccentric changes in circular dichroism of saccharide-linked ethynylpyridine oligomer with copper(II) ions.

Journal: The Journal of organic chemistry20120601

Title: Synthesis and properties of a water-soluble ionic conjugated polymer with carboxylic acids.

Journal: Journal of nanoscience and nanotechnology20120501

Title: Copper(II)/phenanthroline-mediated CD-enhancement and chiral memory effect on a meta-ethynylpyridine oligomer.

Journal: Chemical communications (Cambridge, England)20120404

Title: Synthesis, structural charaterization, and electrochemical and optical properties of ferrocene-triazole-pyridine triads.

Journal: Inorganic chemistry20110905

Title: Synthesis and characterization of a polyacetylene derivative with phenylazobenzene moieties.

Journal: Journal of nanoscience and nanotechnology20110801

Title: Copper(II)-mediated chiral helicity amplification and inversion of meta-ethynylpyridine polymers with metal coordination sites.

Journal: Chemical communications (Cambridge, England)20110714

Title: Potent mGluR5 antagonists: pyridyl and thiazolyl-ethynyl-3,5-disubstituted-phenyl series.

Journal: Bioorganic & medicinal chemistry letters20110601

Title: Hydrogen bond partner reorganization in the coadsorption of a monodendron and pyridylethynyl derivatives.

Journal: Langmuir : the ACS journal of surfaces and colloids20110215

Title: Preparation of ethynylpyridine macrocycles by oxidative coupling of an ethynylpyridine trimer with terminal acetylenes.

Journal: The Journal of organic chemistry20110107

Title: Engineering of linear molecular nanostructures by a hydrogen-bond-mediated modular and flexible host-guest assembly.

Journal: ACS nano20101026

Title: Removal and leakage of environmental tobacco smoke from a model smoking room.

Journal: Journal of occupational and environmental hygiene20101001

Title: Ligand-assisted J-type aggregates of zinc porphyrin: anticooperative molecular organization in self-assembled bolaamphiphile.

Journal: Organic & biomolecular chemistry20100807

Title: Cyclometallated platinum(II) complexes containing pyridyl-acetylide ligands: the selective influence of lead binding on luminescence.

Journal: Dalton transactions (Cambridge, England : 2003)20100121

Title: New 1,2,3-triazole ligands through click reactions and their palladium and platinum complexes.

Journal: Dalton transactions (Cambridge, England : 2003)20091114

Title: 2-[1-(1-Naphth-yl)-1H-1,2,3-triazol-4-yl]pyridine.

Journal: Acta crystallographica. Section E, Structure reports online20090501

Title: 1-(3-Bromo-prop-yl)-4-(2-pyrid-yl)-1H-1,2,3-triazole.

Journal: Acta crystallographica. Section E, Structure reports online20090501

Title: Control of the photoreactivity of diarylethene derivatives by quaternarization of the pyridylethynyl group.

Journal: Organic letters20080515

Title: A new series of dinuclear Au(I) complexes linked by diethynylpyridine groups.

Journal: Dalton transactions (Cambridge, England : 2003)20080328

Title: Helix formation in synthetic polymers by hydrogen bonding with native saccharides in protic media.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20061016

Title: Regulation of saccharide binding with basic poly(ethynylpyridine)s by H+-induced helix formation.

Journal: Journal of the American Chemical Society20051123

Application fold
2-Ethynylpyridine is a chemical compound commonly employed as a versatile building block in organic synthesis. Its molecular structure consists of a pyridine ring with an ethynyl group (-C≡CH) attached to the 2-position, making it highly reactive and suitable for various reactions leading to the formation of diverse organic compounds.

One significant application of 2-ethynylpyridine is in the synthesis of conjugated polymers. Through polymerization reactions, 2-ethynylpyridine can be polymerized to form polymers with unique properties. For example, it can be polymerized to yield poly(2-ethynyl-N-iodopyridinium iodide), poly[2-ethynyl-N-(2-furoyl)pyridinium chloride, and poly[2-ethynyl-N-(propylsulfonate)pyridinium betaine]. These polymers exhibit different functionalities and can find applications in areas such as optoelectronics, materials science, and biomedical engineering.

Additionally, 2-ethynylpyridine can react with various reagents to produce functionalized derivatives. For instance, its reaction with anionic heptaphosphide clusters yields the 4-(2′-pyridyl)-1,2,3-triphospholide anion, which may have applications in coordination chemistry and catalysis.

Moreover, 2-ethynylpyridine can be incorporated into water-soluble ionic conjugated polymers, such as poly[N-(carboxymethyl)-2-ethynylpyridinium bromide], enabling their use in aqueous environments for applications in sensors, drug delivery, and biomedical research.

Furthermore, 2-ethynylpyridine can undergo self-doping reactions to form self-doped ionic conjugated polymers like poly(2-ethynylpyridinimum N-benzoylsulfonate), which possess enhanced conductivity and stability, making them suitable for electronic and optoelectronic applications.

In summary, 2-ethynylpyridine serves as a valuable building block in organic synthesis, enabling the preparation of conjugated polymers and functionalized derivatives with diverse properties and potential applications in various fields of science and technology.
Building Blocks More >
446-52-6
446-52-6
2-Fluorobenzaldehyde
AA003H8M | MFCD00003302
5418-51-9
5418-51-9
5-Nitro-2(1h)-pyridinone
AA003HC7 | MFCD00006276
947-62-6
947-62-6
2-Methoxy-1-naphthoic acid
AA003HFU | MFCD00021532
63012-97-5
63012-97-5
2-Methyl-3-(methylthio)furan
AA003HJJ | MFCD03701635
54677-53-1
54677-53-1
2-Methylpyrrolidine, HCl
AA003HNN | MFCD08274961
26530-20-1
26530-20-1
2-Octylisothiazol-3(2H)-one
AA003HQY | MFCD00072473
6310-21-0
6310-21-0
2-tert-Butylaniline
AA003HUW | MFCD00000794
787591-35-9
787591-35-9
3-(2-Morpholinoethoxy)phenylboronic acid
AA003HYE | MFCD11053818
34071-95-9
34071-95-9
Bolton-hunter reagent
AA003I1T | MFCD00005515
456-46-2
456-46-2
3-(Fluoromethyl)aniline
AA003I5G | MFCD00466952
Submit
© 2017 AA BLOCKS, INC. All rights reserved.