THC & Tropacocaine By Otto Snow

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THC & Tropacocaine
 By Otto Snow

THC & Tropacocaine By Otto Snow


THC & Tropacocaine
 By Otto Snow


Ebook THC & Tropacocaine By Otto Snow

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THC & Tropacocaine
 By Otto Snow

  • Sales Rank: #2517840 in Books
  • Published on: 2004-08-31
  • Original language: English
  • Dimensions: 8.75" h x 6.00" w x .50" l, .70 pounds
  • Binding: Paperback
  • 182 pages

From the Publisher
Book Includes:

Medical Cannabis: CANNABIS. U.S. (Br.) CANNABIS Cannab; THC; Synhexyl Stereochemical Requirements for Cannabimimetic Activity Cannabinoid Receptors CB2 Agonist Treament of Autoimmunine Disorders CB-2 Receptor Agonist Compounds Inhibition of Cell Proliforation; Cannabinoids in the Treatment of Glaucoma Anandamide Amidase Inhibitors as Analgesic Agents CB1 Agonists for Use in Brain Trauma Erratic Gastrointestial Absorbtion of delta-9-Tetrahydrocannabinol Treating Mental Diseases, Inflammation and Pain with Anandamides

Extraction of Delta-9-Tetrahydrocannabinol from Cannabis Extraction of Cannabis Buds (41% THC Oil) Extraction of Cannabis Buds 2 (40% THC Oil) (92% THC Oil) Preparing Delta-9-Tetrahydrocannabinol Reprocessing of the Residue Left After Fractional Distillation of Cannabis Extracts (82% THC Yellow Oil); THC Syntheses Water Soluble Derivatives of Cannabinoids Synthesis of Compound (4) Ketones from Nitriles THC in the Treatment of Glaucoma in Patients who can not take Beta-blockers Compositions useful as a cannabinoid receptor probe Production of 6,12-Dihydro-6-hydroxy-cannabidiol Production of trans-delta-9-Tetrahydrocannabinol Production of 6,12-Dihydro-6-hydroxy-cannabidiol Production of trans-delta-9-Detrahydrocannabinol Preparation of cis-p-Menth-2-ene-1,8,-diol Novel Tetrahydrocannabinol Type Compounds Preparation of (-)-6a,10a-trans-6a,7,8,10a-Tetrahydrodibenzo[b,d]-pyrans Preparation of Optically Active trans-Hexahydrodibenzopyranones 1-Hydroxy-3-(1,1-dimethylheptyl)-6,6-dimethyl-6,6aR,7,8,10,10aR-hexahydro-9-H-dibenzo[b,d]pyran-9-one Producing 6a,10a-trans-6a,7,8,10a-Tetrahydrodibenzo (b,d)-pyrans 3-(1,2-Dimethylheptyl)-6a,7,10,10a-tetra-hydro-1-hydroxy-6,6,9-trimethyl-6H-dibenzo [b,d]pyran

5-Alkylresorcinols: Preparation of l-Hydroxy-2,6-dimethoxy-4-(tertiaryalkyl)benzene 1-Hydroxy-2,6-dimethoxy-4-(1,1-dimethylheptyl)benzene Divarin Dimethyl Ether from 3,4,5-Trimethoxy-propiophenone Reduction of Ketones to Resorcinols Synthesis of 5-Alkylresorcinols; Synthesis of 5-Ethylresorcinol Preparation of Hexylresorcinol by Electrolytic Reduction of Hexanoylresorcinol Synthesis of 5-Methylresorcinol (Orcinol) 5-Alkylresorcinol from Demethylation of 1-(Alkyl)-3,5-Dimethoxybenzene Demethylation Using Pyridine 5-(1,1-dimethylheptyl)resorcinol Demethylation Using 48% Hydrobromic Acid 5-(1,1-Dimethylheptyl)resorcinol ; Preparation of 5-Alkoxyresorcinols Preparation of Phloroglucinol and its Mono-ethers Preparation of Compounds with Marijuana Activity Formation of Tetrahydrocannabinols by Isomerization of Cannabidiol A. By p-toluenesulfonic acid; B. By sulfuric acid; C. By pyridine hydrochloride; D. By phosphoric acid; E. Sulfamic acid; zinc chloride

Converting cis-Hexahydrodibenzo[b,d]pyran-9-ones to trans-Hexahydrodibenzo[b,d]-pyran-9-ones dl-trans-1-Hydroxy-3-(1,1-dimethyl-heptyl) -6,6-dimethyl-6,6a,7,8,10,10a-hexahydro-9H- dibenzo[b,d]pyran-9-one dl-trans-1-Hydroxy-3-n-pentyl-6,6-dimethyl-6,6a,7,8,10,10a-hexahydro-9H-dibenzo[b,d]pyran-9-one dl-trans-1-Hydroxy-3-(1,1-dimethyl-heptyl)-6,6-dimethyl-6,6a,7,8,10,10a-hexahydro-9H-dibenzo[b,d]pyran-9-one Stereoselective Preparation of Hexahydrodibenzopyranones and intermediates (-)-trans-1-Hydroxy-3-(1,1-dimethyl-heptyl)-6,6-dimethyl-6,6a,7,8,10,10a-hexahydro-9H-dibenzo[b,d]pyran-9-one; Acetylation of THC

Delta 1-THC-7-oic acid Analgesic and Anti-inflammatory Agents Platelet Activating Factor Antagonist Non-psychoactive Derivatives of ∆6-THC-7-oic Acid which have Analgesic and Anti-inflammatory Properties Synthesis of (3R,4R)-∆6-THC-DMH-7-oic Acid Acetate

Andanamides: Fatty Acid Amides; Preparation of Arachidonyl Ethanolamide Compounds Isolated from the Brain and Synthesized Synthetic Compounds Prepared and Tested Anandamide Amidase Inhibitors as Analgesic Agents Treating Anxiety and Mood Disorders with Oleamide

Fatty Acid Amides Preparation from Common Household Oils Preparation of Oleamide The Reactions Used N-Substituted Amides of Natural Fatty Acids Preparation of N-Methyl Linseed Oil Fatty Acid Amide Preparation of N-Cyclohexyl Linseed Oil Fatty Acid Amide Preparation of Lauric Diethanolamide from Lauroyl Chloride Preparation of Cocoa Fatty Acid Amide Using the Aminolysis Method

Industrial Manufacture of Fatty Acid Ethanolamides reparation of Oleic Acid Monoethanolamide Purification of Fatty Acid Amides Using Urea Preparation of Olive Oil and Coconut Oil Ethanolamides Preparation of Fatty Acids; Isolation of Linoleic Acid Isolation of Oleic Acid from Olive Oil; Production of Monoalkyolamines

TROPACOCAINE

Coca, The Source of Cocaine; COCAINA. U.S., Br.; COCAINE HYDROCHLORIDUM. U.S., Br. Atropine and the Tropeines Cocaine and the Local Anesthetic; Tropacocaine Benzoyl Ester of Ecgonine Using Benzoic Anhydride Tropacocaine from Pseudo-tropine & Benzoic Anhydride Pseudotropine by Electrolytic Reduction of Tropine Tropineone by Oxidation of Tropine; Extraction of Pseudotropine Pseudotropine by the Electrolytic Reduction of Tropinone Tropinone by the Oxydation of Tropine; Tropinone by the Oxydation of Pseudotropine Tropinone by the Electrolytic Reduction of Tropine or Pseudotropine Benzoic Anhydride

Narcotic Daturas Origin of the Name Jimson, or Jamestown Weed; The Huaca-Cachu of Peru Datura Alkaloids ; Hyoscyamine and Atropine; Atropine Sulphate Hyoscine or Scopolamine ; Extraction of Atropine Growing Datura and Related Species BELLADONNA Atropa belladonna; Atropa belladonna (Belladonna) Cultivation Datura stramonium L. (Jimson Weed) ; Datura stramonium (Jimson weed) Cultivation Hyoscyamus niger (Henbane) Cultivation ; Solanum nigram L. (Black Nightshade)

Anyone interested in the construction and future of CB-1 agonists (eg. THC, Oleamide) or cocaine agonists (eg. tropacocaine) will find this book cutting edge.

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