Bio-Rad Laboratories, Inc. SpectraBase; SpectraBase Compound ID=BKKPE3hEg49
http://spectrabase.com/compound/BKKPE3hEg49 (accessed Sep 15, 2019).

2-Methylpyridine
SpectraBase Compound ID BKKPE3hEg49
InChI InChI=1S/C6H7N/c1-6-4-2-3-5-7-6/h2-5H,1H3
InChIKey BSKHPKMHTQYZBB-UHFFFAOYSA-N
Mol Weight 93.13 g/mol
Molecular Formula C6H7N
Exact Mass 93.057849 g/mol
Copyright Copyright © 1980, 1981-2018 Bio-Rad Laboratories, Inc. All Rights Reserved.
Source of Sample Environmental Protection Agency
Technique NEAT
Copyright Copyright © 1980, 1981-2018 Bio-Rad Laboratories, Inc. All Rights Reserved.
Source of Sample Fluka Chemie AG, Buchs, Switzerland
Technique NEAT
Copyright Copyright © 1980, 1981-2018 Bio-Rad Laboratories, Inc. All Rights Reserved.
Source of Sample The Matheson Company, Inc., Matheson Coleman & Bell
Technique BETWEEN SALTS
Copyright Copyright © 1980, 1981-2018 Bio-Rad Laboratories, Inc. All Rights Reserved.
Source of Sample Allied Corporation
Technique BETWEEN SALTS
Copyright Copyright © 1980, 1981-2018 Bio-Rad Laboratories, Inc. All Rights Reserved.
Source of Sample Fluka Chemie AG, Buchs, Switzerland
Technique CAPILLARY CELL: NEAT
Copyright Copyright © 1991-2018 Bio-Rad Laboratories, Inc. All Rights Reserved.
Source of Sample Fluka AG, Buchs, Switzerland
Solvent CDCl3; Reference=TMS; Temperature 297K
Copyright Copyright © 2009-2018 Bio-Rad Laboratories, Inc. All Rights Reserved.
Source of Sample Fluka Chemie AG, Buchs, Switzerland
Solvent CCl4
Copyright Copyright © 1980, 1981-2018 Bio-Rad Laboratories, Inc. All Rights Reserved.
Copyright Copyright © 1980, 1981-2018 Bio-Rad Laboratories, Inc. All Rights Reserved.
Source of Sample Fluka AG, Buchs, Switzerland
Solvent Chloroform-d; Reference=TMS Spectrometer= Varian HA-100/Digilab FT-NMR-3
Copyright Copyright © 2016 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
Copyright Copyright © 2016 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
Copyright Copyright © 2016 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6
Copyright Copyright © 2016 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Copyright Copyright © 2016 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2018 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO;CR(ACAC)3=0.01M
Copyright Copyright © 2016-2018 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6
Copyright Copyright © 2016-2018 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2018 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2018 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2018 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2018 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2018 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2018 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2018 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 1980, 1981-2018 Bio-Rad Laboratories, Inc. All Rights Reserved.
  • 2-Picoline
  • alpha-PICOLINE
  • alpha-METHYLPYRIDINE
  • 2-PICOLINE;REFERENCE
  • 2-METHYLPYRIDINE;2-PICOLINE
  • BSKHPKMHTQYZBB-UHFFFAOYSA-N
  • 2-METHYL-PYRIDINE;ALPHA-PICOLINE
  • 2-METHYLPYRIDIN
  • 2-PICOLINE (98.7%)
Title Journal or Book Year
Application of multivariate image analysis in modeling 13C-NMR chemical shifts of mono substituted pyridines Magnetic Resonance in Chemistry 2012
A theoretical NMR study of ortho and para-substituted benzenes compared with silabenzenes, pyridines and phosphabenzenes Magnetic Resonance in Chemistry 2010
Experimental and quantum-chemical studies of1H,13C and15N NMR coordination shifts in Au(III), Pd(II) and Pt(II) chloride complexes with picolines Magnetic Resonance in Chemistry 2009
A robust method for determining1H-15N long-range correlations:15N optimized CIGAR-HMBC experiments Magnetic Resonance in Chemistry 2003
Pyridine and aminide derivatives as ligands in 1 : 1 Rh2[tfa]4 adducts:1H,13C and15N NMR study Magnetic Resonance in Chemistry 2003
NMR spectra of nitrogen-containing compounds. Correlations between experimental and GIAO calculated data Magnetic Resonance in Chemistry 1999
Multinuclear NMR spectra of [Pt(L)Cl3]− (L = pyridine derivatives) complexes and crystal structure of trans-Pt(2,6-di(hydroxymethyl)pyridine)2Cl2•2H2O Canadian Journal of Chemistry 1996
Coupling Sign Determination and Isotope-Induced Chemical Shifts1Δ15/14N(29Si),1Δ15/14N(119Sn) and1Δ29/28Si(15N): Multinuclear Magnetic Resonance Study ofN-Trimethylsilyl-, -stannyl- and -plumbyl-Substituted 2-Aminopyridines, 2,6-Diaminopyridines and Analogous 2-Picolines Magnetic Resonance in Chemistry 1996
15N NMR spectroscopy of some azines Organic Magnetic Resonance 1984
Structures of pyridines obtained in the aluminum bromide mediated cyclocongregation of acetylenes with cyanoformates The Journal of Organic Chemistry 1984
Carbon-13 chemical shifts of some pyridines, 2,2'-bipyridyls and 1,10-phenanthrolines Australian Journal of Chemistry 1978
Long range13C1H coupling constants. III—methylpyridines Organic Magnetic Resonance 1975