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3- Isopropyl-2,4-dimethylpentane

Dimethylpentane Isopropyl benzene fraMS-2-Pentene 1,2,4-Trimethylbenzene... [Pg.169]

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]

UN 1206, see 3,3-Dimethylpentane Heptane UN 1208, see 2,2-Dimethylbutane, 2,3-Dimethylbutane, Hexane, 2-Methylpentane UN 1212, see Isobutyl alcohol UN 1213, see Isobutyl acetate UN 1218, see 2-Methyl-l,3-butadiene UN 1220, see Isopropyl acetate UN 1221, see Isopropylamine UN 1224, see 3-Heptanone, 2-Hexanone, Isophorone UN 1229, see Mesityl oxide UN 1230, see Methanol UN 1231, see Methyl acetate UN 1232, see 2-Butanone UN 1233, see sec-Hexyl acetate... [Pg.1514]

Ketonic hydrolysis to di-isopropyl ketone. Mix 14 g (0.75 mol) of the ester with 30 ml of glacial acetic acid, 10 ml of water and 10 ml of concentrated sulphuric acid, and boil under reflux until evolution of carbon dioxide ceases. Dilute the cooled solution with 180 ml of water, add 100 ml of ether and render alkaline to phenolphthalein with 20 per cent sodium hydroxide solution. Separate the ether layer, extract the aqueous layer with two 50 ml portions of ether, dry the combined ether layer and extracts with anhydrous sodium sulphate, distil off the ether and fractionate the residue. The yield of di-isopropyl ketone (2,4-dimethylpentan-3-one), b.p. 123-124 °C, is 6.5 g (76%). [Pg.742]

Synonym diisopropyloxyde, isopropyl ether, 2-isopropoxypropane, 2,2-oxybispropane, 3-oxa-2,4-dimethylpentane, IPE, DIPE... [Pg.29]

Table 12 also indicates the manner in which propyl, butyl, and pentyl carbon units prefer to be added to the bridgehead of adamantane. Although the isopropyl unit is more highly branched than the n-propyl unit, l-(2-propyl)-adamantane possesses four skew interactions whereas the l-(l-pn yl)-adamantane derivative has a minimum energy conformation with only two skews, and is calculated to have a small energy advantage. A similar advantage is held for 1-propyl (A///. -49.20 kcal mole" (2Sb)) over 2-propyl AH. —48.87 kcal mole" (25A)) when t-butyl is substituted for 1-adamantyl that is, 2,2-dimethylpentane is more stable than 2,2,3-trimethylbutane. [Pg.81]

Similarly, the gauche conformations as lowest-energy forms were observed in 2,3-dimethylpentane and 3,4-dimethylhexane . For the methyl carbon atoms of the isopropyl group in 2,4-dimethylhexane 28 a chemical shift difference of 1.5 ppm is... [Pg.371]

See other pages where 3- Isopropyl-2,4-dimethylpentane is mentioned: [Pg.42]    [Pg.155]    [Pg.1291]    [Pg.42]    [Pg.106]    [Pg.1336]    [Pg.42]    [Pg.155]    [Pg.1336]    [Pg.460]    [Pg.25]    [Pg.1291]    [Pg.33]    [Pg.42]    [Pg.1266]    [Pg.660]    [Pg.160]    [Pg.106]   
See also in sourсe #XX -- [ Pg.154 ]

See also in sourсe #XX -- [ Pg.154 ]



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2.3- Dimethylpentane

3.3- Dimethylpentan

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