L-Isopropyl-3-

Indazole, 5,5-dimethyl-3-trifluoromethyl-4,5-dihydro-trichomonacidal activity, 5, 291 Indazole, 2-ethoxycarbonyl-reactions, 5, 269 Indazole, 3-fluoro-synthesis, S, 263 Indazole, 1-germyl-synthesis, 5, 236 Indazole, 1-glycosyl-synthesis, 5, 289 Indazole, 2-glycosyl-synthesis, 5, 289 Indazole, halo-reactions, S, 266 Indazole, 2-hydroxy-methylation, 5, 269 Indazole, 3-hydroxy-reactions, S, 264 Indazole, 6-hydroxy-diazo coupling, 5, 86 Indazole, hydroxyphenyl-synthesis, S, 288 Indazole, 3-iodo-synthesis, S, 241 Indazole, l-isopropyl-3-phenyl-reduction, 5, 243 Indazole, 3-mercapto-1 -substituted tautomerism, 5, 265 Indazole, methoxy-... 

The major metabolite of buprofezin in plants is its p-hydroxy metabolite (p-OH-buprofezin) and that in soil is l-isopropyl-3-phenylurea (BF12). The target analytes are considered to be buprofezin and p-OH-buprofezin in plant materials, buprofezin and BF12 in soils and buprofezin in water samples. 

Generation of (/t)-l-Lithio-l-methoxymethnxy-2-methylpropane (5 b) and Alkylation to (4,5,5,S)-4,5-Diiso-propyl-2- (I.V,2.V)-l-isopropyl-3-methyl-2-mcthoxymethoxybutyl -l,3,2-dioxaborolane (6b) Typical Procedure29 ... 

Ring closure to a bicyclic product could also be expected in the irradiation of peril uoroazacyclohexadiene 25, but the product obtained, in 87% yield, is peril uoro[l-isopropyl-3-(methylimino)cyclobutene] (27), which is presumed to be formed via ring opening to azatriene 26, followed by electrocyclic ring closure to the cyclobutene and a 1,3-fluorine shift.20... 

Sodium bis(2-methoxyethoxy)aluminum hydride (S)-6-Fluoro-l-isopropyl-3,4-dihydro-lH-naphthalen-2-one... 

To the mixture 22.7 g (0.54 mol) dry lithium chloride and 100 mL THF at -15°C was added 160 mL 2 molar lithium diisopropylamide (0.32 mol) in heptane/THF/ethylbenzene was added. Then a solution of 36.6 g (0.16 mol) N-[3-(lH-benzimidazol-2-yl)-propyl]-N-methylacetamide in 140 mL toluene was added, the solution was stirred for 2 hours, and a further 155 mL toluene was added. (S)-6-Fluoro-l-isopropyl-3,4-dihydro-lH-naphthalen-2-one (29.9 g, 0.15 mol), in 15 mL toluene was added. After stirring at -10°C for 4 hours, the resulting solution was added to 200 mL ice water. The pH of the resulting mixture was adjusted to 7-8 by addition of a 71 g concentrated hydrochloric acid. The organic layer washed with water, then the solvents removed under reduced pressure to give 96 g of (lS,2S)-N-[3-(lH-benzimidazol-2-yl)propyl]-... 

Azetidin l-Isopropyl-3-methansulfo-nyloxy- E16c, 885 (O-Sulfonier.) Piperidinium 1-Ethyl-l-sulfo- Xl/2,... 

Acetamino-2,5-dimethyl-l-isopropyl-3-oxo- E16b, 214 (2-Oxo-l,2-dihydro-pyridin)... 

There is an isopropyl group at carbon 1 and a methyl group at carbon 3. The name is l-isopropyl-3-methylcyclohexane, since the alkyl groups are named in alphabetical order. 

DIMETHYL-a-IONONE see COW780 a-a-DIMETHYL-m-ISOPROPENYL BENZYL ISOCYANATE see IKG800 DIMETHYL-5-(l-ISOPROPYL-3-METHYLPYR, ZOLYL)CARBAMATE see DSK200... 

Heating of a solution of purec/s-2-benzoyl-l-isopropyl-3-(m-nitrophenyl)aziridine (7) in dry acetonitrile under reflux for 24 hours gave 1,2-diisopropyl-2,5-diphenyl-... 

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