Ethyl isobutyl sulfide

A = 13363 CsHi602 CsHisS Ethyl Caproate Isobutyl sulfide 167.7 172.0 Nonazeotrope 256... [Pg.230]

Ethylaniline /i-Octyl alcohol j c-Octyl alcohol Butyl sulfide Isobutyl sulfide Benzyl ethyl ether... [Pg.359]

Ethyl vinyl sulfide Isopropyl methyl sulfide Methyl n-propyl sulfide leri-Butyl methyl sulfide Chloromethyl methyl sulfide Ethyl isopropyl sulfide Isobutyl methyl sulfide Methyl 2-methylallyl sulfide Allyl ethyl sulfide Ethyl n-propyl sulfide... [Pg.420]

Ethyl Acetoacetate continued) o-Chloro toluene p-Chloro toluene Anisole o-Cresol Styrene Acetophenone Phenyl acetate m-Xylene o-Xylene p-Xylene p-Methylanisole Phenetole Veratrole Methylheptenone Butyl butyrate Isoamyl propionate Butyl ether sec-Octyl alcohol Butyl sulfide Isobutyl sulfide Indene Mesitylene Propylbenzene Pseudocumene Benzyl ethyl ether... [Pg.176]

Xylidine Ethyl fumarate Ethyl maleate Methylheptenone Ethyl succinate 2-Octanone Isoamyl lactate Octyl alcohol S6c-0ctyl alcohol Butyl sulfide Isobutyl sulfide Ethyl silicate Indene... [Pg.205]

Ethyl sulfide ( CijH, c,S ) + Acetic acid ( CjHijOj ) Lecat, 1949 Isobutyl sulfide ( CgH,gS ) + Butyric acid ( C HgOg ) Lecat, 1949... [Pg.456]

Ethyl, isobutyl, and phenyl vinyl sulfide behave as typical good electron-donating monomers, readily undergoing alternative copolymerization with a strong electron acceptor such as Vinyl sulfide-MA mixtures... [Pg.386]

The reductive alkylation of /V-alkylarylamines and diarylamine with ketones to give tertiary amines has been investigated by Greenfield and Malz, Jr.42 with platinum metal sulfides that had been shown to be excellent catalysts for the reductive alkylation of primary arylamines with ketones37 (see eq. 6.15). Good conversions to tertiary amines were obtained with relatively unhindered secondary arylamines and less hindered ketones. The relative ease in the reductive alkylation of diarylamines with ketones was in the following order cyclohexanone > acetone > ethyl methyl ketone > isoamyl methyl ketone > isobutyl methyl ketone. For example, 58% of diphenylamine was converted to iV-alkyldiphenylamine with cyclohexanone over rhodium sulfide at 150°C and 3.4-5.5 MPa H2 (eq. 6.19), while with isobutyl methyl ketone, a conversion of only 28% was obtained even at 235°C with in the same reaction time. [Pg.245]

Butyl alcohol aec-Butyl alcohol tert-Butyl alcohol Isobutyl alcohol Ethyl sulfide... [Pg.120]

Ethyl butyrate Ethyl isobutyrate Isoamyl formate Isobutyl acetate Methyl isovalerate Propyl propionate Paraldehyde Isopropyl sulfide Ethyl borate Toluene... [Pg.286]

Potassium amyl xanthate Potassium ethyl xanthate Sodium isobutyl xanthate Sodium isopropyl xanthate flotation collector, gold ore Sodium di-s-butyl dithiophosphate flotation collector, iron sulfide Ammonium dibutyl dithiophosphate flotation collector, lead Ammonium dibutyl dithiophosphate Sodium diethyidithiocarbamate... [Pg.5295]

Isobutyl nitrite Butyl alcohol scc-Butyl alcohol t r -Butyl alcohol Ethyl ether Isobutyl alcohol Ethyl sulfide Pyridine Isovaleraldehyde 3-Methyl 2-butanone Isobutyl formate Isopropyl acetate Methyl isobutyrate Isoamyl nitrite tert-Amyl alcohol Isoamyl alcohol... [Pg.16]

Isopropyl alcohol Butyl alcohol aec-Butyl alcohol Isobutyl alcohol Cyclopentanol Butyl formate Methyl butyrate Propyl acetate Amyl alcohol (art-Amyl alcohol Isoamyl alcohol 2-Pentanol Allyl sulfide Ethyl butyrate Ethyl isobutyrate Isobutyl acetate Propyl sulfide Isopropyl sulfide Ethyl borate Toluene... [Pg.73]

Isobutyl alcohol Ethyl sulfide Cyclopentane 2-Methyl-2-butene 3>Pentanone Isobutyl formate Methyl isobutyrate Propyl acetate l-Bromo-3-methylbutane... [Pg.127]

Linalool o -Terpineol /8-Terpineol Propyl succinate Citronellol Menthol Capric acid Ethyl caprylate Isoamyl isovalerate n-Decyl alcohol Isoamyl sulfide Isobutyl benzoate Terpineol methyl ether Ethyl pelargonate Isoamyl carbonate 1,3,5-Triethylbenzene Bornyl acetate Bornyl ethyl ether Tridecane... [Pg.239]