1945-84-2 | 2-Ethynylpyridine

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$8.00	$6.00
5g	95%	in stock	$27.00	$19.00
10g	95%	in stock	$45.00	$32.00
25g	95%	in stock	$111.00	$78.00
100g	95%	in stock	$443.00	$311.00

Description

• Catalog Number: AB62099
• Chemical Name: 2-Ethynylpyridine
• CAS Number: 1945-84-2
• Molecular Formula: C7H5N
• Molecular Weight: 103.1213
• MDL Number: MFCD00041598
• SMILES: C#Cc1ccccn1

Computed Properties

• Complexity: 109
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 1

Literature

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

  Dalton transactions (Cambridge, England : 2003) 20121107

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

  Organic & biomolecular chemistry 20120914

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

  The Journal of organic chemistry 20120601

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

  Journal of nanoscience and nanotechnology 20120501

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

  Chemical communications (Cambridge, England) 20120404

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

  Inorganic chemistry 20110905

• Synthesis and characterization of a polyacetylene derivative with phenylazobenzene moieties.

  Journal of nanoscience and nanotechnology 20110801

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

  Chemical communications (Cambridge, England) 20110714

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

  Bioorganic & medicinal chemistry letters 20110601

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

  Langmuir : the ACS journal of surfaces and colloids 20110215

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

  The Journal of organic chemistry 20110107

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

  ACS nano 20101026

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

  Journal of occupational and environmental hygiene 20101001

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

  Organic & biomolecular chemistry 20100807

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

  Dalton transactions (Cambridge, England : 2003) 20100121

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

  Dalton transactions (Cambridge, England : 2003) 20091114

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

  Acta crystallographica. Section E, Structure reports online 20090501

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

  Acta crystallographica. Section E, Structure reports online 20090501

• Control of the photoreactivity of diarylethene derivatives by quaternarization of the pyridylethynyl group.

  Organic letters 20080515

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

  Dalton transactions (Cambridge, England : 2003) 20080328

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

  Chemistry (Weinheim an der Bergstrasse, Germany) 20061016

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

  Journal of the American Chemical Society 20051123