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3- methyl-4-propyl-3-octene

Substituents 3-methyl and 4-propyl Name 3-Methyl-4-propyl-3-octene... [Pg.331]

EINECS 203-468-6, see Ethylenediamine EINECS 203-470-7, see Allyl alcohol EINECS 203-472-8, see Chloroacetaldehyde EINECS 203-481-7, see Methyl formate EINECS 203-523-4, see 2-Methylpentane EINECS 203-528-1, see 2-Pentanone EINECS 203-544-9, see 1-Nitropropane EINECS 203-545-4, see Vinyl acetate EINECS 203-548-0, see 2,4-Dimethylpentane EINECS 203-550-1, see 4-Methyl-2-pentanone EINECS 203-558-5, see Diisopropylamine EINECS 203-560-6, see Isopropyl ether EINECS 203-561-1, see Isopropyl acetate EINECS 203-564-8, see Acetic anhydride EINECS 203-571-6, see Maleic anhydride EINECS 203-576-3, see m-Xylene EINECS 203-598-3, see Bis(2-chloroisopropyl) ether EINECS 203-604-4, see 1,3,5-Trimethylbenzene EINECS 203-608-6, see 1,3,5-Trichlorobenzene EINECS 203-620-1, see Diisobutyl ketone EINECS 203-621-7, see sec-Hexyl acetate EINECS 203-623-8, see Bromobenzene EINECS 203-624-3, see Methylcyclohexane EINECS 203-625-9, see Toluene EINECS 203-628-5, see Chlorobenzene EINECS 203-630-6, see Cyclohexanol EINECS 203-632-7, see Phenol EINECS 203-686-1, see Propyl acetate EINECS 203-692-4, see Pentane EINECS 203-694-5, see 1-Pentene EINECS 203-695-0, see cis-2-Pentene EINECS 203-699-2, see Butylamine EINECS 203-713-7, see Methyl cellosolve EINECS 203-714-2, see Methylal EINECS 203-716-3, see Diethylamine EINECS 203-721-0, see Ethyl formate EINECS 203-726-8, see Tetrahydrofuran EINECS 203-729-4, see Thiophene EINECS 203-767-1, see 2-Heptanone EINECS 203-772-9, see Methyl cellosolve acetate EINECS 203-777-6, see Hexane EINECS 203-799-6, see 2-Chloroethyl vinyl ether EINECS 203-804-1, see 2-Ethoxyethanol EINECS 203-806-2, see Cyclohexane EINECS 203-807-8, see Cyclohexene EINECS 203-809-9, see Pyridine EINECS 203-815-1, see Morpholine EINECS 203-839-2, see 2-Ethoxyethyl acetate EINECS 203-870-1, see Bis(2-chloroethyl) ether EINECS 203-892-1, see Octane EINECS 203-893-7, see 1-Octene EINECS 203-905-0, see 2-Butoxyethanol EINECS 203-913-4, see Nonane EINECS 203-920-2, see Bis(2-chloroethoxy)methane EINECS 203-967-9, see Dodecane EINECS 204-066-3, see 2-Methylpropene EINECS 204-112-2, see Triphenyl phosphate EINECS 204-211-0, see Bis(2-ethylhexyl) phthalate EINECS 204-258-7, see l,3-Dichloro-5,5-dimethylhydantoin... [Pg.1482]

The oxidation and double bond isomerization are competitive reactions, and the extents of these reactions are influenced by solvents. DMF is good for the oxidation, whereas use of acetic acid facilitates the isomerization. Both reactions proceed in alcoholic solvents. Acetonitrile and DMSO retard oxidation by complex formation with the catalysts. The double bond migration is facilitated by high temperatures. The oxidation of 1-octene in n-propyl alcohol yielded 2-octanone to the extent of 62% at 90 °C, 85% at 60 C, and more than 97% at 30 °C. 4-Methyl-1-pentene isomerized to the 2- and 3-alkenes, which formed ir-allylic complexes in ethanol, but normal oxidation to the methyl ketone took place in DMF and y-butyrolactone. ... [Pg.451]

Octen l-Hydroxy-7-methyl- E21d, 3350 ([3.3]-sigmatr. Rearrangem.) Oxetan 2-Propyl-3,3,4-trimethyl-IV/5b, 842... [Pg.676]

P2B02PtC4oH57, Platinum(II). (3-methoxy-3-oxo-KO-propyl-KC )bis(triethylphos-phine)-, tetraphenylborate(l-), 26 138 P2BPtC44Ht3, Platinum(ll), (q -cyclo-octene)bis(triethylphosphine)-, tetra-phenylborate( 1 —), 26 139 P2C4H 4, Phosphine, 12-ethanediylbis(di-methyl-, nickel complex, 28 101 P2C25H22. Phosphine, methylenebis(di-phenyl-, palladium complex, 28 340 ruthenium complex, 26 276,28 225 P2C26H20, Phosphine, ethynnediylbis(di-phenyl-, ruthenium complex, 26 277, 28 226... [Pg.405]

Acetaldehyde phenethyl propyl acetal Acetic acid, (cyclohexyloxy)-, 2-propenyl ester Allyl phenoxyacetate Amyl benzoate Bicycle [2.2.2]-5-octene-2-carboxylic acid, 1(or 4)-methyl-4(or 1)-(1-methylethyl) methyl ester Bornyl acetate... [Pg.5326]

The cyclopalladation of allylic or homoallylic amines and sulfides proceeds due to the chelating effect of N and S atoms, and has been used for functionalization of alkenes. For example, i-propyl 3-butenyl sulfide is carbopalladated with methyl cy-clopentanecarboxylate and Li2PdCl4. Reduction of the chelated complex with sodium cyanoborohydride affords the alkylated keto ester in 96% yield (eq 24). Functionalization of 3-N,N-dimethylaminocyclopentene for the synthesis of a prostaglandin skeleton has been carried out via a IV-chelated palladium complex as an intermediate. In the first step, malonate was introduced regio- and stereoselectively by carbopalladation (eq 25). Elimination of a /3-hydrogen generated a new cyclopentene, and its oxypalladation with 2-chloroethanol, followed by insertion of 1-octen-3-one and /3-elimination, afforded the final product. [Pg.502]

See other pages where 3- methyl-4-propyl-3-octene is mentioned: [Pg.2298]    [Pg.251]    [Pg.372]    [Pg.44]    [Pg.1040]    [Pg.44]    [Pg.344]    [Pg.286]    [Pg.7056]    [Pg.521]    [Pg.170]   
See also in sourсe #XX -- [ Pg.332 ]

See also in sourсe #XX -- [ Pg.332 ]



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1- octen

1-Octene

2- Methyl-4-octene

5-Methyl-2-propyl

Methyl propylate

Octenal

Octenes

Octenes 1-octene

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