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s-Triazines and derivatives [[electronic resource] /] / Edwin M. Smolin and Lorence Rapoport
s-Triazines and derivatives [[electronic resource] /] / Edwin M. Smolin and Lorence Rapoport
Autore Smolin Edwin M
Pubbl/distr/stampa New York, : Interscience Publishers, 1959
Descrizione fisica 1 online resource (670 p.)
Disciplina 547
547/.59/05
Altri autori (Persone) RapoportLorence <1919-1999.>
Collana The chemistry of heterocyclic compounds
Soggetto topico Triazines
Heterocyclic compounds
ISBN 1-282-30147-0
9786612301476
0-470-18662-3
0-470-18812-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto s-Triazines and Derivatives; Contents; Introduction; I. General; II. s-Triazine; 1. General; 2. Synthesis; 3. Reactions; A. Salt Formation; B. Hydrolysis; C. Reaction with Hydrogen Chloride; D. Reaction with Amines; E. Reaction with Halogens; F. Reaction with Sodamide; G. Hydrogenation; H. Friedel-Crafts Reaction of s-Triazine and Its Hydrochloride Derivatives; I. Grignard Reaction; I. Cyanuric Acid and Derivatives; I. Introduction; II. Cyanuric Acid; 1. Historical; 2. Physical Properties; A. General; B. Density; C. Thermal Properties; D. Heat of Neutralization; E. Dissociation Constant
F. Percentage Dissociated at 35°G. Conductivity; H. Viscosity and Density of Solutions; I. Specific Heat; J. Magnetic Susceptibility; K. Raman, Infrared, and Ultraviolet Spectra; L. Polarographic Behavior; M. Crystallography and Miscellaneous Properties; 3. Synthesis and Occurrence; A. Natural Occurrence; B. From Cyanuric Halides; C. Polymerization of Cyanic Acid; D. From Urea and Urea Derivatives; E. From Uric Acid; F. From Allophanates and Carbamyl Chlorides; G. From Carbonyl Diurethane and Carbethoxybiuret; H. From Formamide Electrolytically; I. From Acetoxamide
J. From Carbaminothioglycolic Acid AnilideK. Miscellaneous Preparations; 4. Structure; 5. Salts of Cyanuric Acid; 6. Reactions of Cyanuric Acid; A. Hydrolysis; B. Reaction with Active Halogen Compounds; C. Thermal Action; D. Reaction with Ammonia; E. Esterification; F. Acetylation; G. Reaction with Fatty Acids; H. Reaction with α-Haloacids; I. Rearrangement .; 7. Applications of Cyanuric Acid; A. Physiological and Technical Significance; B. Melamine Formation; C. Rubber Manufacture; D. Resins; III. Cyanuric Halides; 1. Cyanuric Chloride; A. History; B. Physical Properties
C. Synthetic Methods(1) From Cyanogen Chloride; (2) From Hydrocyanic Acid; (3) From Cyanuric Acid; (4) Miscellaneous Methods; D. Structure; E. Reactions; (1) Hydrolysis and Alcoholysis; (2) Reaction with Hydroxy Compounds; (3) Reaction with Amino Compounds; (4) Reaction with Sulfhydryl Compounds; (5) Reaction with Salts of Hydrazoic Acid; (6) Reaction with Silver Nitrate; (7) Grignard Reaction; (8) Wurtz-Fittig Reaction; (9) Friedel-Crafts Reaction; (10) Reaction with Carboxylic Acids and Salts; (11) Reaction with Malonic Ester; (12) Reaction with Hydriodic Acid; (13) Reduction
(14) Reaction with BenzamideF. Physiological Properties; 2. Cyanuric Bromide; A. Synthesis; (1) Polymerization of Cyanogen Bromide; (2) From Bromine and Potassium Ferrocyanide; B. Reactions and Structure; (1) Hydrolysis; (2) Reaction with Amines; (3) With Acetic Acid; (4) Reaction with Urea; 3. Cyanuric Iodide; 4. Cyanuric Fluoride; 5. 2-Bromo-4,6-dichloro-s-triazine; 6. 2-Chloro-4,6-diiodo-s-triazine; IV. Cyanuric Acid Esters; 1. Alkyl Esters; A. Methyl Esters; (1) Trimethyl Ester; (2) Diethyl Ester; (3) Halomethoxy-s-triazines; (4) Mixed Methyl Esters; B. Ethyl Esters; (1) Triethyl Ester
(2) Dimethyl Ester
Record Nr. UNINA-9910144287703321
Smolin Edwin M  
New York, : Interscience Publishers, 1959
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
s-Triazines and derivatives [[electronic resource] /] / Edwin M. Smolin and Lorence Rapoport
s-Triazines and derivatives [[electronic resource] /] / Edwin M. Smolin and Lorence Rapoport
Autore Smolin Edwin M
Pubbl/distr/stampa New York, : Interscience Publishers, 1959
Descrizione fisica 1 online resource (670 p.)
Disciplina 547
547/.59/05
Altri autori (Persone) RapoportLorence <1919-1999.>
Collana The chemistry of heterocyclic compounds
Soggetto topico Triazines
Heterocyclic compounds
ISBN 1-282-30147-0
9786612301476
0-470-18662-3
0-470-18812-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto s-Triazines and Derivatives; Contents; Introduction; I. General; II. s-Triazine; 1. General; 2. Synthesis; 3. Reactions; A. Salt Formation; B. Hydrolysis; C. Reaction with Hydrogen Chloride; D. Reaction with Amines; E. Reaction with Halogens; F. Reaction with Sodamide; G. Hydrogenation; H. Friedel-Crafts Reaction of s-Triazine and Its Hydrochloride Derivatives; I. Grignard Reaction; I. Cyanuric Acid and Derivatives; I. Introduction; II. Cyanuric Acid; 1. Historical; 2. Physical Properties; A. General; B. Density; C. Thermal Properties; D. Heat of Neutralization; E. Dissociation Constant
F. Percentage Dissociated at 35°G. Conductivity; H. Viscosity and Density of Solutions; I. Specific Heat; J. Magnetic Susceptibility; K. Raman, Infrared, and Ultraviolet Spectra; L. Polarographic Behavior; M. Crystallography and Miscellaneous Properties; 3. Synthesis and Occurrence; A. Natural Occurrence; B. From Cyanuric Halides; C. Polymerization of Cyanic Acid; D. From Urea and Urea Derivatives; E. From Uric Acid; F. From Allophanates and Carbamyl Chlorides; G. From Carbonyl Diurethane and Carbethoxybiuret; H. From Formamide Electrolytically; I. From Acetoxamide
J. From Carbaminothioglycolic Acid AnilideK. Miscellaneous Preparations; 4. Structure; 5. Salts of Cyanuric Acid; 6. Reactions of Cyanuric Acid; A. Hydrolysis; B. Reaction with Active Halogen Compounds; C. Thermal Action; D. Reaction with Ammonia; E. Esterification; F. Acetylation; G. Reaction with Fatty Acids; H. Reaction with α-Haloacids; I. Rearrangement .; 7. Applications of Cyanuric Acid; A. Physiological and Technical Significance; B. Melamine Formation; C. Rubber Manufacture; D. Resins; III. Cyanuric Halides; 1. Cyanuric Chloride; A. History; B. Physical Properties
C. Synthetic Methods(1) From Cyanogen Chloride; (2) From Hydrocyanic Acid; (3) From Cyanuric Acid; (4) Miscellaneous Methods; D. Structure; E. Reactions; (1) Hydrolysis and Alcoholysis; (2) Reaction with Hydroxy Compounds; (3) Reaction with Amino Compounds; (4) Reaction with Sulfhydryl Compounds; (5) Reaction with Salts of Hydrazoic Acid; (6) Reaction with Silver Nitrate; (7) Grignard Reaction; (8) Wurtz-Fittig Reaction; (9) Friedel-Crafts Reaction; (10) Reaction with Carboxylic Acids and Salts; (11) Reaction with Malonic Ester; (12) Reaction with Hydriodic Acid; (13) Reduction
(14) Reaction with BenzamideF. Physiological Properties; 2. Cyanuric Bromide; A. Synthesis; (1) Polymerization of Cyanogen Bromide; (2) From Bromine and Potassium Ferrocyanide; B. Reactions and Structure; (1) Hydrolysis; (2) Reaction with Amines; (3) With Acetic Acid; (4) Reaction with Urea; 3. Cyanuric Iodide; 4. Cyanuric Fluoride; 5. 2-Bromo-4,6-dichloro-s-triazine; 6. 2-Chloro-4,6-diiodo-s-triazine; IV. Cyanuric Acid Esters; 1. Alkyl Esters; A. Methyl Esters; (1) Trimethyl Ester; (2) Diethyl Ester; (3) Halomethoxy-s-triazines; (4) Mixed Methyl Esters; B. Ethyl Esters; (1) Triethyl Ester
(2) Dimethyl Ester
Record Nr. UNISA-996202934803316
Smolin Edwin M  
New York, : Interscience Publishers, 1959
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
s-Triazines and derivatives [[electronic resource] /] / Edwin M. Smolin and Lorence Rapoport
s-Triazines and derivatives [[electronic resource] /] / Edwin M. Smolin and Lorence Rapoport
Autore Smolin Edwin M
Pubbl/distr/stampa New York, : Interscience Publishers, 1959
Descrizione fisica 1 online resource (670 p.)
Disciplina 547
547/.59/05
Altri autori (Persone) RapoportLorence <1919-1999.>
Collana The chemistry of heterocyclic compounds
Soggetto topico Triazines
Heterocyclic compounds
ISBN 1-282-30147-0
9786612301476
0-470-18662-3
0-470-18812-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto s-Triazines and Derivatives; Contents; Introduction; I. General; II. s-Triazine; 1. General; 2. Synthesis; 3. Reactions; A. Salt Formation; B. Hydrolysis; C. Reaction with Hydrogen Chloride; D. Reaction with Amines; E. Reaction with Halogens; F. Reaction with Sodamide; G. Hydrogenation; H. Friedel-Crafts Reaction of s-Triazine and Its Hydrochloride Derivatives; I. Grignard Reaction; I. Cyanuric Acid and Derivatives; I. Introduction; II. Cyanuric Acid; 1. Historical; 2. Physical Properties; A. General; B. Density; C. Thermal Properties; D. Heat of Neutralization; E. Dissociation Constant
F. Percentage Dissociated at 35°G. Conductivity; H. Viscosity and Density of Solutions; I. Specific Heat; J. Magnetic Susceptibility; K. Raman, Infrared, and Ultraviolet Spectra; L. Polarographic Behavior; M. Crystallography and Miscellaneous Properties; 3. Synthesis and Occurrence; A. Natural Occurrence; B. From Cyanuric Halides; C. Polymerization of Cyanic Acid; D. From Urea and Urea Derivatives; E. From Uric Acid; F. From Allophanates and Carbamyl Chlorides; G. From Carbonyl Diurethane and Carbethoxybiuret; H. From Formamide Electrolytically; I. From Acetoxamide
J. From Carbaminothioglycolic Acid AnilideK. Miscellaneous Preparations; 4. Structure; 5. Salts of Cyanuric Acid; 6. Reactions of Cyanuric Acid; A. Hydrolysis; B. Reaction with Active Halogen Compounds; C. Thermal Action; D. Reaction with Ammonia; E. Esterification; F. Acetylation; G. Reaction with Fatty Acids; H. Reaction with α-Haloacids; I. Rearrangement .; 7. Applications of Cyanuric Acid; A. Physiological and Technical Significance; B. Melamine Formation; C. Rubber Manufacture; D. Resins; III. Cyanuric Halides; 1. Cyanuric Chloride; A. History; B. Physical Properties
C. Synthetic Methods(1) From Cyanogen Chloride; (2) From Hydrocyanic Acid; (3) From Cyanuric Acid; (4) Miscellaneous Methods; D. Structure; E. Reactions; (1) Hydrolysis and Alcoholysis; (2) Reaction with Hydroxy Compounds; (3) Reaction with Amino Compounds; (4) Reaction with Sulfhydryl Compounds; (5) Reaction with Salts of Hydrazoic Acid; (6) Reaction with Silver Nitrate; (7) Grignard Reaction; (8) Wurtz-Fittig Reaction; (9) Friedel-Crafts Reaction; (10) Reaction with Carboxylic Acids and Salts; (11) Reaction with Malonic Ester; (12) Reaction with Hydriodic Acid; (13) Reduction
(14) Reaction with BenzamideF. Physiological Properties; 2. Cyanuric Bromide; A. Synthesis; (1) Polymerization of Cyanogen Bromide; (2) From Bromine and Potassium Ferrocyanide; B. Reactions and Structure; (1) Hydrolysis; (2) Reaction with Amines; (3) With Acetic Acid; (4) Reaction with Urea; 3. Cyanuric Iodide; 4. Cyanuric Fluoride; 5. 2-Bromo-4,6-dichloro-s-triazine; 6. 2-Chloro-4,6-diiodo-s-triazine; IV. Cyanuric Acid Esters; 1. Alkyl Esters; A. Methyl Esters; (1) Trimethyl Ester; (2) Diethyl Ester; (3) Halomethoxy-s-triazines; (4) Mixed Methyl Esters; B. Ethyl Esters; (1) Triethyl Ester
(2) Dimethyl Ester
Record Nr. UNINA-9910829891003321
Smolin Edwin M  
New York, : Interscience Publishers, 1959
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
s-Triazines and derivatives / / Edwin M. Smolin and Lorence Rapoport
s-Triazines and derivatives / / Edwin M. Smolin and Lorence Rapoport
Autore Smolin Edwin M
Pubbl/distr/stampa New York, : Interscience Publishers, 1959
Descrizione fisica 1 online resource (670 p.)
Disciplina 547
547/.59/05
Altri autori (Persone) RapoportLorence <1919-1999.>
Collana The chemistry of heterocyclic compounds
Soggetto topico Triazines
Heterocyclic compounds
ISBN 1-282-30147-0
9786612301476
0-470-18662-3
0-470-18812-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto s-Triazines and Derivatives; Contents; Introduction; I. General; II. s-Triazine; 1. General; 2. Synthesis; 3. Reactions; A. Salt Formation; B. Hydrolysis; C. Reaction with Hydrogen Chloride; D. Reaction with Amines; E. Reaction with Halogens; F. Reaction with Sodamide; G. Hydrogenation; H. Friedel-Crafts Reaction of s-Triazine and Its Hydrochloride Derivatives; I. Grignard Reaction; I. Cyanuric Acid and Derivatives; I. Introduction; II. Cyanuric Acid; 1. Historical; 2. Physical Properties; A. General; B. Density; C. Thermal Properties; D. Heat of Neutralization; E. Dissociation Constant
F. Percentage Dissociated at 35°G. Conductivity; H. Viscosity and Density of Solutions; I. Specific Heat; J. Magnetic Susceptibility; K. Raman, Infrared, and Ultraviolet Spectra; L. Polarographic Behavior; M. Crystallography and Miscellaneous Properties; 3. Synthesis and Occurrence; A. Natural Occurrence; B. From Cyanuric Halides; C. Polymerization of Cyanic Acid; D. From Urea and Urea Derivatives; E. From Uric Acid; F. From Allophanates and Carbamyl Chlorides; G. From Carbonyl Diurethane and Carbethoxybiuret; H. From Formamide Electrolytically; I. From Acetoxamide
J. From Carbaminothioglycolic Acid AnilideK. Miscellaneous Preparations; 4. Structure; 5. Salts of Cyanuric Acid; 6. Reactions of Cyanuric Acid; A. Hydrolysis; B. Reaction with Active Halogen Compounds; C. Thermal Action; D. Reaction with Ammonia; E. Esterification; F. Acetylation; G. Reaction with Fatty Acids; H. Reaction with α-Haloacids; I. Rearrangement .; 7. Applications of Cyanuric Acid; A. Physiological and Technical Significance; B. Melamine Formation; C. Rubber Manufacture; D. Resins; III. Cyanuric Halides; 1. Cyanuric Chloride; A. History; B. Physical Properties
C. Synthetic Methods(1) From Cyanogen Chloride; (2) From Hydrocyanic Acid; (3) From Cyanuric Acid; (4) Miscellaneous Methods; D. Structure; E. Reactions; (1) Hydrolysis and Alcoholysis; (2) Reaction with Hydroxy Compounds; (3) Reaction with Amino Compounds; (4) Reaction with Sulfhydryl Compounds; (5) Reaction with Salts of Hydrazoic Acid; (6) Reaction with Silver Nitrate; (7) Grignard Reaction; (8) Wurtz-Fittig Reaction; (9) Friedel-Crafts Reaction; (10) Reaction with Carboxylic Acids and Salts; (11) Reaction with Malonic Ester; (12) Reaction with Hydriodic Acid; (13) Reduction
(14) Reaction with BenzamideF. Physiological Properties; 2. Cyanuric Bromide; A. Synthesis; (1) Polymerization of Cyanogen Bromide; (2) From Bromine and Potassium Ferrocyanide; B. Reactions and Structure; (1) Hydrolysis; (2) Reaction with Amines; (3) With Acetic Acid; (4) Reaction with Urea; 3. Cyanuric Iodide; 4. Cyanuric Fluoride; 5. 2-Bromo-4,6-dichloro-s-triazine; 6. 2-Chloro-4,6-diiodo-s-triazine; IV. Cyanuric Acid Esters; 1. Alkyl Esters; A. Methyl Esters; (1) Trimethyl Ester; (2) Diethyl Ester; (3) Halomethoxy-s-triazines; (4) Mixed Methyl Esters; B. Ethyl Esters; (1) Triethyl Ester
(2) Dimethyl Ester
Record Nr. UNINA-9910876692503321
Smolin Edwin M  
New York, : Interscience Publishers, 1959
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui