Chemistry of Heterocyclic Compounds: Pyridine and its Derivatives, Part Three, Volume 14

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Refractive index n D. Dipole moment.

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Threshold limit value. LD 50 median dose. LC 50 median concentration. PEL Permissible. REL Recommended. IDLH Immediate danger. Related amines. Structure and properties. Spectral data. General form of the pyridinium cation.

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Part 5, Volume 14 | Introduction and Scope Synthesis of AnneIated Pyridines Chemistry of Heterocyclic Compounds: Pyridine and its Derivatives, Part 5, .. A Shortened Synthesis Of 4-(3-Aminopropyl) Pyrazole, An Affinity Ligand For. Pyridine and Its Derivatives, Part 3 (Chemistry of Heterocyclic Compounds: A . the editor of Pyridine and Its Derivatives, Part 3, Volume 14, published by Wiley.

Cambridge: The Royal Society of Chemistry. Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. Thieme Chemistry. Stuttgart: Georg Thieme. Oxford: Blackwell Scientific Publications. Journal of Physical and Chemical Reference Data. Journal of the American Chemical Society. Organometallchemie 6th ed. Reviews of Modern Physics. Bibcode : RvMP The Journal of Chemical Physics.

Bibcode : JChPh.. IARC Monographs Aromatic Heterocyclic Chemistry. Oxford University Press. EDP Sciences. Pyridine and its Derivatives. New York: Interscience. Transactions of the Royal Society of Edinburgh. Annalen der Chemie und Pharmacie in German. Part II". From p. Chemical News. Bulletin for the History of Chemistry. Lectures on the history of the development of chemistry since the time of Lavoisier.

Heterocyclic Chemistry. Berichte der Deutschen Chemischen Gesellschaft in German. Ladenburg, A. Philosophical Magazine. Henninger, aus Paris.

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April ". Berichte der Deutschen Chemischen Gesellschaft Correspondence. Berichte der Deutschen Chemischen Gesellschaft. Ueber eine Erweiterung der Hantzsch'schen Dihydropyridinsynthese" [Syntheses in the pyridine series. On an extension of the Hantzsch dihydropyridine synthesis]. Fenaroli's Handbook of Flavor Ingredients. Lebensmittel-Lexikon 4th ed. Journal of Agricultural and Food Chemistry. Food and Chemical Toxicology.

In Moskowitz, Howard R. Odor Quality and Chemical Structure. Journal of Periodontology Research. A Study of the Chichibabin Synthesis". Angewandte homogene Katalyse. Part III. Reaction of pyrroles with dichlorocarbene". Journal of the Chemical Society C: Organic 18 : Tetrahedron Letters. Chemische Berichte.

Institute of Chemistry, Skopje. Archived from the original on 16 June Biochemical Journal. Plant Physiology.

US5103011A - Preparation of 2-chloro-5- methyl-pyridine - Google Patents

Campaigne Acta Chemica Scandinavica. The Journal of Organic Chemistry. Norris; Riechers, E. Advances in Heterocyclic Chemistry. Organic Syntheses. Archived from the original PDF on 21 January Thermochemistry of Organic and Organometallic Compounds. New York: Academic Press. Journal of Organometallic Chemistry.

Collection of Czechoslovak Chemical Communications. Infrared and Raman spectra of Inorganic and Coordination compounds. Part A 5th ed. Part B 5th ed. Accounts of Chemical Research. Geneva: World Health Organization. In Paquette, L. Encyclopedia of Reagents for Organic Synthesis. New York: J. Jena University. Archived from the original PDF on 19 July Oxidation of alcohols to aldehydes and ketones: a guide to current common practice.

New York: Springer. Retrieved 8 October Environmental Protection Agency. Alfa Aesar. Retrieved 3 June SI Chemical Data 6th ed. Retrieved 17 January Fiche Toxicologique in French. Environmental Toxicology and Chemistry. Applied and Environmental Microbiology. Environ Sci Technol. Bibcode : EnST J; Traina, S. Bibcode : Chmsp Pure and Applied Chemistry. Die systematische Nomenklatur der Organischen Chemie 4th ed. Berlin: Springer. Functional groups. Phosphonate Phosphonous. Selenol Selenonic acid Seleninic acid Selenenic acid Selone. Tellurol Telluroketone. Isothiocyanate Phosphoramide Sulfenyl chloride Sulfonamide Thiocyanate.

See also chemical classification , chemical nomenclature inorganic , organic. Categories : Pyridines Amine solvents Foul-smelling chemicals Aromatic bases Simple aromatic rings Functional groups Aromatic solvents. Namespaces Article Talk. Views Read Edit View history. In other projects Wikimedia Commons.

By using this site, you agree to the Terms of Use and Privacy Policy. Other names Azine Azabenzene. EC Number. Colorless liquid [2]. Nauseating, fish-like [3]. See: data page. R-phrases outdated. Explosive limits. Lethal dose or concentration LD, LC :. Picoline Quinoline.

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