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The Organic Chemist's Desk Reference has been essential reading for laboratory chemists who need a succinct guide to the fundamentals of organic chemistry. Extensively revised and updated, this new edition contains the very latest data that chemists need access to for experimentation and research.
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The Organic Chemist's Desk Reference has been essential reading for laboratory chemists who need a succinct guide to the fundamentals of organic chemistry. Extensively revised and updated, this new edition contains the very latest data that chemists need access to for experimentation and research.
Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Produktdetails
- Produktdetails
- Verlag: Taylor & Francis Ltd (Sales)
- 3rd edition
- Seitenzahl: 296
- Erscheinungstermin: 9. August 2017
- Englisch
- Abmessung: 251mm x 175mm x 18mm
- Gewicht: 544g
- ISBN-13: 9781498734011
- ISBN-10: 1498734014
- Artikelnr.: 48746288
- Verlag: Taylor & Francis Ltd (Sales)
- 3rd edition
- Seitenzahl: 296
- Erscheinungstermin: 9. August 2017
- Englisch
- Abmessung: 251mm x 175mm x 18mm
- Gewicht: 544g
- ISBN-13: 9781498734011
- ISBN-10: 1498734014
- Artikelnr.: 48746288
Cooper, Caroline; Purchase, Rupert
The Organic Chemistry Literature. Abstracting and Other Current Awareness
Services. Principal Electronic Dictionaries. Useful Reference Works and
Review Series. Patents, Including Patent Awareness Services.
Cheminformatics Companies. Primary Journals. Endnotes. Nomenclature
Fundamentals . IUPAC Nomenclature. CAS Nomenclature. Types of Name.
Constructing a Systematic Name. Nomenclature of Ring Systems. Ring Systems
(General). Bridged Ring Systems. Spiro Compounds. Heterocyclic Ring
Systems. Ring Assemblies. Ring Fusion Names. Nomenclature of Individual
Classes of Compound. Carbohydrates. Alditols and Cyclitols. Amino Acids and
Peptides. Natural Products (General). Steroids. Lipids. Carotenoids.
Lignans. Nucleotides and Nucleosides. Tetrapyrroles. Organoboron Compounds.
Organophosphorus (and Organoarsenic) Compounds. Azo and Azoxy Compounds.
Labelled Compounds. Tautomeric Compounds. Acronyms and Miscellaneous Terms
Used in Describing Organic Molecules. Abbreviations and Acronyms for
Reagents and Protecting Groups in Organic Chemistry. Glossary of
Miscellaneous Terms and Techniques Used in Nomenclature, Including
Colloquial Terms. Stereochemistry. The Sequence Rule: R and S. Graphical
and Textual Representations of Stereochemistry. Chiral Molecules with No
Centres of Chirality. E and Z. The D,L-System. Descriptors and Terms Used
in Stereochemistry. Graphical Representation of Organic Compounds. Zigzag
Natta Projection. Stereochemistry. CAS Numbers, InChI, and Other
Identifiers. CAS Registry Numbers. InChI. Simplified Molecular Input Line
Entry System (SMILES). Molecular Formulae. The Hill System. Chemical
Abstracts Conventions.Checking Molecular Formulae. Chemical Hazard
Information for the Laboratory. Hazard and Risk Assessment. Physical and
Reactive Chemical Hazards. Health Hazards. Handling and Storage of
Chemicals. Hazardous Reaction Mixtures. Disposal of Chemicals. Solvents.
Peroxide- Forming Chemicals. Further Literature Sources. Spectroscopy.
Infrared Spectroscopy. Ultraviolet Spectroscopy. Nuclear Magnetic Resonance
Spectroscopy. Mass Spectrometry. Introduction. Ionisation Techniques and
Mass Spectrometer Systems. Interpreting Mass Spectra and Molecular Mass.
Sample Introduction and Solvent Systems for Electrospray Mass Spectrometry.
Common Adducts and Contaminants in Mass Spectra. MALDI Matrices. Fragment
Ions and Neutral Losses. Natural Abundance and Isotopic Masses of Selected
Isotopes and Nuclear Particles. Glossary of Abbreviations and Terms
Commonly Used in Mass Spectrometry. Crystallography. Introduction.
Definitions.Crystallographic Point Groups. Space Groups. Reciprocal
Lattice. Examples of Organic Crystals. CIF Data Format. Bragg's Law and the
X-Ray Spectrum. Crystal Specimen Preparation for X-Ray Analysis.
Chromatographic Chiral Separation. Types of Molecular Interactions.
Diastereomeric Compounds and Complexes. Chiral Mobile Phases. Chiral
Stationary Phases. Laboratory Data and SI Units. Solvents. Buffer
Solutions. Acid and Base Dissociation Constants. Resolving Agents. Freezing
Mixtures. Materials Used for Heating Baths. Drying Agents.
Pressure-Temperature Nomograph. SI Units. Languages. A German-English
Dictionary. Russian and Greek Alphabets. SI Units. Index
Services. Principal Electronic Dictionaries. Useful Reference Works and
Review Series. Patents, Including Patent Awareness Services.
Cheminformatics Companies. Primary Journals. Endnotes. Nomenclature
Fundamentals . IUPAC Nomenclature. CAS Nomenclature. Types of Name.
Constructing a Systematic Name. Nomenclature of Ring Systems. Ring Systems
(General). Bridged Ring Systems. Spiro Compounds. Heterocyclic Ring
Systems. Ring Assemblies. Ring Fusion Names. Nomenclature of Individual
Classes of Compound. Carbohydrates. Alditols and Cyclitols. Amino Acids and
Peptides. Natural Products (General). Steroids. Lipids. Carotenoids.
Lignans. Nucleotides and Nucleosides. Tetrapyrroles. Organoboron Compounds.
Organophosphorus (and Organoarsenic) Compounds. Azo and Azoxy Compounds.
Labelled Compounds. Tautomeric Compounds. Acronyms and Miscellaneous Terms
Used in Describing Organic Molecules. Abbreviations and Acronyms for
Reagents and Protecting Groups in Organic Chemistry. Glossary of
Miscellaneous Terms and Techniques Used in Nomenclature, Including
Colloquial Terms. Stereochemistry. The Sequence Rule: R and S. Graphical
and Textual Representations of Stereochemistry. Chiral Molecules with No
Centres of Chirality. E and Z. The D,L-System. Descriptors and Terms Used
in Stereochemistry. Graphical Representation of Organic Compounds. Zigzag
Natta Projection. Stereochemistry. CAS Numbers, InChI, and Other
Identifiers. CAS Registry Numbers. InChI. Simplified Molecular Input Line
Entry System (SMILES). Molecular Formulae. The Hill System. Chemical
Abstracts Conventions.Checking Molecular Formulae. Chemical Hazard
Information for the Laboratory. Hazard and Risk Assessment. Physical and
Reactive Chemical Hazards. Health Hazards. Handling and Storage of
Chemicals. Hazardous Reaction Mixtures. Disposal of Chemicals. Solvents.
Peroxide- Forming Chemicals. Further Literature Sources. Spectroscopy.
Infrared Spectroscopy. Ultraviolet Spectroscopy. Nuclear Magnetic Resonance
Spectroscopy. Mass Spectrometry. Introduction. Ionisation Techniques and
Mass Spectrometer Systems. Interpreting Mass Spectra and Molecular Mass.
Sample Introduction and Solvent Systems for Electrospray Mass Spectrometry.
Common Adducts and Contaminants in Mass Spectra. MALDI Matrices. Fragment
Ions and Neutral Losses. Natural Abundance and Isotopic Masses of Selected
Isotopes and Nuclear Particles. Glossary of Abbreviations and Terms
Commonly Used in Mass Spectrometry. Crystallography. Introduction.
Definitions.Crystallographic Point Groups. Space Groups. Reciprocal
Lattice. Examples of Organic Crystals. CIF Data Format. Bragg's Law and the
X-Ray Spectrum. Crystal Specimen Preparation for X-Ray Analysis.
Chromatographic Chiral Separation. Types of Molecular Interactions.
Diastereomeric Compounds and Complexes. Chiral Mobile Phases. Chiral
Stationary Phases. Laboratory Data and SI Units. Solvents. Buffer
Solutions. Acid and Base Dissociation Constants. Resolving Agents. Freezing
Mixtures. Materials Used for Heating Baths. Drying Agents.
Pressure-Temperature Nomograph. SI Units. Languages. A German-English
Dictionary. Russian and Greek Alphabets. SI Units. Index
The Organic Chemistry Literature. Abstracting and Other Current Awareness
Services. Principal Electronic Dictionaries. Useful Reference Works and
Review Series. Patents, Including Patent Awareness Services.
Cheminformatics Companies. Primary Journals. Endnotes. Nomenclature
Fundamentals . IUPAC Nomenclature. CAS Nomenclature. Types of Name.
Constructing a Systematic Name. Nomenclature of Ring Systems. Ring Systems
(General). Bridged Ring Systems. Spiro Compounds. Heterocyclic Ring
Systems. Ring Assemblies. Ring Fusion Names. Nomenclature of Individual
Classes of Compound. Carbohydrates. Alditols and Cyclitols. Amino Acids and
Peptides. Natural Products (General). Steroids. Lipids. Carotenoids.
Lignans. Nucleotides and Nucleosides. Tetrapyrroles. Organoboron Compounds.
Organophosphorus (and Organoarsenic) Compounds. Azo and Azoxy Compounds.
Labelled Compounds. Tautomeric Compounds. Acronyms and Miscellaneous Terms
Used in Describing Organic Molecules. Abbreviations and Acronyms for
Reagents and Protecting Groups in Organic Chemistry. Glossary of
Miscellaneous Terms and Techniques Used in Nomenclature, Including
Colloquial Terms. Stereochemistry. The Sequence Rule: R and S. Graphical
and Textual Representations of Stereochemistry. Chiral Molecules with No
Centres of Chirality. E and Z. The D,L-System. Descriptors and Terms Used
in Stereochemistry. Graphical Representation of Organic Compounds. Zigzag
Natta Projection. Stereochemistry. CAS Numbers, InChI, and Other
Identifiers. CAS Registry Numbers. InChI. Simplified Molecular Input Line
Entry System (SMILES). Molecular Formulae. The Hill System. Chemical
Abstracts Conventions.Checking Molecular Formulae. Chemical Hazard
Information for the Laboratory. Hazard and Risk Assessment. Physical and
Reactive Chemical Hazards. Health Hazards. Handling and Storage of
Chemicals. Hazardous Reaction Mixtures. Disposal of Chemicals. Solvents.
Peroxide- Forming Chemicals. Further Literature Sources. Spectroscopy.
Infrared Spectroscopy. Ultraviolet Spectroscopy. Nuclear Magnetic Resonance
Spectroscopy. Mass Spectrometry. Introduction. Ionisation Techniques and
Mass Spectrometer Systems. Interpreting Mass Spectra and Molecular Mass.
Sample Introduction and Solvent Systems for Electrospray Mass Spectrometry.
Common Adducts and Contaminants in Mass Spectra. MALDI Matrices. Fragment
Ions and Neutral Losses. Natural Abundance and Isotopic Masses of Selected
Isotopes and Nuclear Particles. Glossary of Abbreviations and Terms
Commonly Used in Mass Spectrometry. Crystallography. Introduction.
Definitions.Crystallographic Point Groups. Space Groups. Reciprocal
Lattice. Examples of Organic Crystals. CIF Data Format. Bragg's Law and the
X-Ray Spectrum. Crystal Specimen Preparation for X-Ray Analysis.
Chromatographic Chiral Separation. Types of Molecular Interactions.
Diastereomeric Compounds and Complexes. Chiral Mobile Phases. Chiral
Stationary Phases. Laboratory Data and SI Units. Solvents. Buffer
Solutions. Acid and Base Dissociation Constants. Resolving Agents. Freezing
Mixtures. Materials Used for Heating Baths. Drying Agents.
Pressure-Temperature Nomograph. SI Units. Languages. A German-English
Dictionary. Russian and Greek Alphabets. SI Units. Index
Services. Principal Electronic Dictionaries. Useful Reference Works and
Review Series. Patents, Including Patent Awareness Services.
Cheminformatics Companies. Primary Journals. Endnotes. Nomenclature
Fundamentals . IUPAC Nomenclature. CAS Nomenclature. Types of Name.
Constructing a Systematic Name. Nomenclature of Ring Systems. Ring Systems
(General). Bridged Ring Systems. Spiro Compounds. Heterocyclic Ring
Systems. Ring Assemblies. Ring Fusion Names. Nomenclature of Individual
Classes of Compound. Carbohydrates. Alditols and Cyclitols. Amino Acids and
Peptides. Natural Products (General). Steroids. Lipids. Carotenoids.
Lignans. Nucleotides and Nucleosides. Tetrapyrroles. Organoboron Compounds.
Organophosphorus (and Organoarsenic) Compounds. Azo and Azoxy Compounds.
Labelled Compounds. Tautomeric Compounds. Acronyms and Miscellaneous Terms
Used in Describing Organic Molecules. Abbreviations and Acronyms for
Reagents and Protecting Groups in Organic Chemistry. Glossary of
Miscellaneous Terms and Techniques Used in Nomenclature, Including
Colloquial Terms. Stereochemistry. The Sequence Rule: R and S. Graphical
and Textual Representations of Stereochemistry. Chiral Molecules with No
Centres of Chirality. E and Z. The D,L-System. Descriptors and Terms Used
in Stereochemistry. Graphical Representation of Organic Compounds. Zigzag
Natta Projection. Stereochemistry. CAS Numbers, InChI, and Other
Identifiers. CAS Registry Numbers. InChI. Simplified Molecular Input Line
Entry System (SMILES). Molecular Formulae. The Hill System. Chemical
Abstracts Conventions.Checking Molecular Formulae. Chemical Hazard
Information for the Laboratory. Hazard and Risk Assessment. Physical and
Reactive Chemical Hazards. Health Hazards. Handling and Storage of
Chemicals. Hazardous Reaction Mixtures. Disposal of Chemicals. Solvents.
Peroxide- Forming Chemicals. Further Literature Sources. Spectroscopy.
Infrared Spectroscopy. Ultraviolet Spectroscopy. Nuclear Magnetic Resonance
Spectroscopy. Mass Spectrometry. Introduction. Ionisation Techniques and
Mass Spectrometer Systems. Interpreting Mass Spectra and Molecular Mass.
Sample Introduction and Solvent Systems for Electrospray Mass Spectrometry.
Common Adducts and Contaminants in Mass Spectra. MALDI Matrices. Fragment
Ions and Neutral Losses. Natural Abundance and Isotopic Masses of Selected
Isotopes and Nuclear Particles. Glossary of Abbreviations and Terms
Commonly Used in Mass Spectrometry. Crystallography. Introduction.
Definitions.Crystallographic Point Groups. Space Groups. Reciprocal
Lattice. Examples of Organic Crystals. CIF Data Format. Bragg's Law and the
X-Ray Spectrum. Crystal Specimen Preparation for X-Ray Analysis.
Chromatographic Chiral Separation. Types of Molecular Interactions.
Diastereomeric Compounds and Complexes. Chiral Mobile Phases. Chiral
Stationary Phases. Laboratory Data and SI Units. Solvents. Buffer
Solutions. Acid and Base Dissociation Constants. Resolving Agents. Freezing
Mixtures. Materials Used for Heating Baths. Drying Agents.
Pressure-Temperature Nomograph. SI Units. Languages. A German-English
Dictionary. Russian and Greek Alphabets. SI Units. Index