MARC details
| 000 -LEADER |
|---|
| fixed length control field |
07145nam a22002777i 4500 |
| 005 - DATE AND TIME OF LATEST TRANSACTION |
|---|
| control field |
20200922143729.0 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION |
|---|
| fixed length control field |
200218s2018 ii a|||| |||| 001 0 eng d |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
|---|
| International Standard Book Number |
9789387085145 |
| 040 ## - CATALOGING SOURCE |
|---|
| Original cataloging agency |
EG-NcFUE |
| Description conventions |
rda |
| 082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER |
|---|
| Edition number |
23 |
| Classification number |
615.19 |
| Item number |
S.A.O |
| 100 1# - MAIN ENTRY--PERSONAL NAME |
|---|
| Personal name |
Siddiqui, Anees Ahmad |
| 245 10 - TITLE STATEMENT |
|---|
| Title |
Organic Medicinal Chemistry : |
| Remainder of title |
practical Manual for Pharmacy and Science Students / |
| Statement of responsibility, etc |
Anees Ahmad Siddiqui. |
| 250 ## - EDITION STATEMENT |
|---|
| Edition statement |
First Edition. |
| 264 #1 - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT) |
|---|
| Place of publication, distribution, etc |
New Delhi : |
| Name of publisher, distributor, etc |
CBS Publishers & Distiributors, |
| Date of publication, distribution, etc |
2018. |
| 300 ## - PHYSICAL DESCRIPTION |
|---|
| Extent |
254 Pages : |
| Other physical details |
illustraions ; |
| Dimensions |
24 cm. |
| 336 ## - CONTENT TYPE |
|---|
| Source |
rdacontent |
| Content type term |
text |
| 337 ## - MEDIA TYPE |
|---|
| Source |
rdamedia |
| Media type term |
unmediated |
| 338 ## - CARRIER TYPE |
|---|
| Source |
rdacarrier |
| Carrier type term |
volume |
| 500 ## - GENERAL NOTE |
|---|
| General note |
Includes Index. |
| 505 0# - FORMATTED CONTENTS NOTE |
|---|
| Formatted contents note |
BASIC CHEMISTRY LAB EQUIPMENT Heating Devices -- Magnetic Stirrer -- Fumehood -- COMMON LABORATORY TECHNIQUES Handling of Glassware -- Heating Sources -- Filtration -- Decolourization -- Refluxing -- Sublimation -- Chromatography -- Solvent Drying and Drying Agents -- Use of Conventional Drying Agents -- Drying Process of Some Common Solvents -- TRAPS -- Simple Distillation -- Calculation of Percent Yield -- Theoretical, Actual and Percent Yields -- 3. CRYSTALLIZATION TECHNIQUE Selection of a Suitable Solvent for the Recrystallization -- Dissolving the Impure Solid in a Minimum Volume of Hot Solvent -- Removal of Any Insoluble Impurities by Filtration -- Crystallization of the Desired Compound from the Solution -- Isolation of the Purified Solid Compound -- DETERMINATION OF MELTING AND BOILING POINTS Determination of Melting Point -- Determination of Boiling Point -- SINGLE STEP SYNTHESIS -- |
| 505 0# - FORMATTED CONTENTS NOTE |
|---|
| Formatted contents note |
Experiment 5.1: Synthesis of Aspirin (Acetyl Salicylic Acid) from Salicylic Acid -- Experiment 5.2: Synthesis of 2,4,6-Tribromophenol from Phenol -- Experiment 5.3: Synthesis of Picric Acid from Phenol -- Experiment 5.4: Synthesis of Urotropine from Formaldehyde -- Experiment 5.5: Synthesis of Phenyl Benzoate from Phen? -- Experiment 5.6: Synthesis of 2,3-Dihydro-1,4-Phthalazinedione from Phthalic Anhydride -- Experiment 5.7: Synthesis of Methyl Salicylate (Oil of Wintergreen) from Salicylic Acid -- Experiment 5.8: Synthesis of m-Dinitrobenzene from Nitrobenzene -- Experiment 5.9: Synthesis of Dibenzalacetone from Acetone -- Experiment 5.10: Synthesis of 2,4,6-Tribromoaniline from Aniline -- Experiment 5.11: Synthesis of 1,2,3,4-Tetrahydrocarbazole from Cyclohexanone -- Experiment 5.12: Synthesis of 7-Hydroxycoumarin (Umbelliferone) -- Experiment 5.13: Synthesis of 2,4,5-Triphenyl IH-Imidazole from Benzil -- Experiment 5,14: Synthesis of Benzylideneaniline (Schiff Base) from Aniline -- Experiment 5.15: Synthesis of 2-Naphthol Aniline or Aniline Yellow Dye -- Experiment 5.16: Synthesis of lodoform from Ethyl Alcohol or Acetone -- Experiment 5.17: Synthesis of Benzoic Acid from Benzamide -- xperiment 5.18: Synthesis of Benztriazole from o-Phenylenediamine -- Experiment 5.19: Synthesis of Benzimidazole from o-Phenylenediamine -- Experiment 5.20: Synthesis of 2-Phenyl-4H-Benzo[1,3] Oxazin-4-one from Anthranilic Acıd -- Experiment 5.21: Synthesis of 3,5-Dimethyl Pyrazole from Acetylacetone -- Experiment 5.22: Synthesis of 2,5-Diphenyl Oxazole -- Experiment 5.23: Synthesis of Chalcone (Benzal Acetophenone) -- Experiment 5.24: Synthesis of m-Nitrobenzoic Acid from Benzoic Acid -- Experiment 5.25: Synthesis of Barbituric Acid from Urea -- Experiment 5.26: Synthesis of a-Phenylthiourea from Aniline --Experiment 5.27: Synthesis of Glucosazone from Glucose -- Experiment 5.28: Synthesis of Anthrone from Anthraquinone -- Experiment 5.29: Synthesis of Phenolphthalein from Phthalic Anhydride and Phenol -- Experiment 5.30: Synthesis of Benzocaine from para-Aminobenzoic Acid -- Experiment 5.31: Synthesis of Benzanilide from Aniline -- Experiment 5.32: Synthesis of Chlorobutanol from Acetone and Chloroform -- Experiment 5.33: Synthesis of Acetaminophen from p-Aminophenol -- Experiment 5.34: Synthesis of Phenothiazine from Diphenylamine -- Experiment 5.35: Synthesis of Phenacetin from Acetaminophen -- Experiment 5.36: Synthesis of 1-Phenyl-3-Methylpyrazol-5-one from Phenyl Hydrazine -- Experiment 5.37: Synthesis of Hippuric Acid from Glycine -- Experiment 5.38: Synthesis of 2,5-Dimethyl-1-Phenyl Pyrole from 2,5-Hexanedione I17 Experiment 5.39: Synthesis of Benzoic Acid (and Benzyl Alcohol) from Benzaldehyde -- Experiment 5.40: Synthesis of 5-Nitro Salicylic Acid from Salicylic Acid --Experiment 5.41: Synthesis of Cinnamic Acid from Benzaldehyde -- 6. TWO STEP SYNTHESIS Experiment -- 6.1: Synthesis of p-Bromoacetanilide from Aniline -- Experiment 6.2: Synthesis of p-Nitroacetanilide from Aniline -- Experiment 6.3: Synthesis of 4-Methyl-7-Acetoxycoumarin from Resorcinol -- Experiment 6.4: Synthesis of 9-Acridone from o-Chlorobenzoic Acid -- Experiment 6.5: Synthesis of 4-Benzylidene-2-Methyloxazole-5-one from Glycine -- Experiment 6.6: Synthesis of Dilantin (5,5-Diphenyl Hydantoin) from Benzoin -- Experiment 6.7: Synthesis of Anthranilic Acid from Phthalic Anhydride -- Experiment 6.8: Synthesis of 2-Phenylindole from Acetophenone -- Experiment 6.9: Synthesis of Benzilic Acid from Benzoin -- Experiment 6.10: Synthesis of 2,3-Diphenyl Quinoxaline from Benzil and b-Phenylenediamine -- Experiment 6.11: Synthesis of 6-Methoxy-2-Amino Benzothiazole from 6-Methoxy-2-Aniline -- Experiment 6.12: Synthesis of 4-Phenyl Butyric Acid from Benzene via Friedel Craft Reaction -- Experiment 6.13: Synthesis of Caprolactam from Cyclohexanone -- Experiment 6.14: Synthesis of Propranalol from a-Naphthol -- Experiment 6.15: Synthesis of Isatin from Aniline -- Experiment 6.16: Synthesis of Lidocaine from 2,6-Dimethyl Aniline -- Experiment 6.17: Synthesis of Methyl Orange from Aniline -- Experiment 6.18: Synthesis of Eosin from Resorcinol -- 7. MULTI STEP SYNTHESIS -- Experiment 7.1: Synthesis of Flavone from 2-Hydroxy Acetophenone -- Experiment 7.2: Synthesis of p-Bromoaniline from Aniline -- Experiment 7.3: Synthesis of Sulphanilamide from Aniline -- Experiment 7.4: Synthesis of N-Phenyl Succinimide from Succinic Acid -- Experiment 7.5: Synthesis of Tolbutamide from Toluene -- 8. EXTRACTION PROCEDURE -- Experiment 8.1: Extraction of Caffeine from Tea Leaves -- Experiment 8.2: Isolation of L-Cystine from Human Hairs -- Experiment 8.3: Extraction of Carvone from Caraway Seeds -- Experiment 8.4: Isolation of Limonene from Orange Peel -- Experiment 8.5: Isolation of Eugenol from Clove Buds -- Experiment 8.6: Isolation of Citric Acid from Lemon Juice -- Experiment 8.7: Isolation of Nicotine from Tobacco Leaves -- Experiment 8.8: Isolation of Piperine froh Pepper -- Experiment 8.9: Extraction of Casein from Milk -- Experiment 8.10: Isolation of Lactose from Powdered Milk -- Experiment 8.11: Isolation of Lycopene from Tomato -- Experiment 8.12: Isolation of Trimyristin from Nutmeg -- Experiment 8.13: Isolation of Quercetin from the Leaves of Fenugreek (Trigonella Foenum) -- SECTION III 9. ORGANIC NAME REACTIONS -- VIVA VOCE QUESTIONS -- INDEX |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
|---|
| Topical term or geographic name as entry element |
Chemistry, Organic. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
|---|
| Topical term or geographic name as entry element |
Pharmaceutical chemistry |
| 942 ## - ADDED ENTRY ELEMENTS (KOHA) |
|---|
| Source of classification or shelving scheme |
Dewey Decimal Classification |
| Koha item type |
Books |