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1,2,3-Triazole as a safer and practical substitute for cyanide in the Bruylants reaction for the synthesis of tertiary amines containing tertiary alkyl or aryl groups. Tetrahedron Letters 2005 , 46 (33) , 5455-5458.
- Asher Kalir, Habib Edery, Zvi Pelah, D. Balderman, Gila Porath
- 1969
Step 3: 1-phenylcyclohexylamine (PCA): To a cooled solution of 198 gm of KOH in 1 L of water was added 18 mL of bromine, and the solution further cooled to 7 C. 67.3 gm (0.331 mole) of 1-phenylcyclohexanecarboxamide was added at once, and the mixture held at 3-9 C for 90 min. with stirring. It was then extracted 3 times with 200 mL of ether ...
Feb 6, 2010 · IUPAC Standard InChI: InChI=1S/C12H17N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1,3-4,7-8,12-13H,2,5-6,9-10H2 Copy IUPAC Standard InChIKey: TXTHKGMZDDTZFD-UHFFFAOYSA-N ...
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Apr 2, 2013 · Drug Testing and Analysis is a specialist journal covering sports doping, recreational drugs, pharmaceuticals, toxico-pathology, forensics, and the environment.
- Jason Wallach, Giorgia De Paoli, Adeboye Adejare, Simon D. Brandt
- 2014
administered subcutaneously to mice and gerbils, and 0.2 m1/100 g to rats. Monkeys were injected (0.25 ml/kg) into the saphena vein. In cats the maximal volume injected was 0.2 ml. In all cases the animals used were of either sex. Hydrochlorides of 5 10 1 8 3 4 6 8 3 10 10 10 10 10 10 10 1 2 6 0 44 10 0 7 60 100 25 0 0 0 0 0 0 25 100 5 10 2 5 7
Feb 13, 2019 · William Reusch, Professor Emeritus ( Michigan State U. ), Virtual Textbook of Organic Chemistry. 10.10: An Introduction to Multiple Step Synthesis. Integrating the different reactions from the first 10 chapters of this text into multiple step synthetic pathways is an important skill in mastering organic chemistry.
Data from NIST Standard Reference Database 69: NIST Chemistry WebBook The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment.
