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Hexyl-methyl

Place 80 g, of hydroxylamine sulphate (or 68-5 g. of the hydrochloride), 25 g. of hydrated sodium acetate, and 100 ml. of water in a 500 ml. flask fitted with a stirrer and a reflux water-condenser, and heat the stirred solution to 55-60°. Run in 35 g (42 nil,) of -hexyl methyl ketone, and continue the heating and vigorous stirring for ij hours. (The mixture can conveniently be set aside overnight after this stage.) Extract the oily oxime from the cold mixture twice with ether. Wash the united ethereal extract once with a small quantity of water, and dry it with sodium sulphate. Then distil off the ether from the filtered extract, preferably using a distillation flask of type shown in Fig. 41 (p. 65) and of ca, 50 ml, capacity, the extract being run in as fast as the ether distils, and then fractionally distil the oxime at water-pump pressure. Collect the liquid ketoxime, b.p. 110-111713 mm. Yield, 30-32 g. [Pg.225]

Substitutive lUPAC name 1 Methoxyhexane Functional class name Hexyl methyl ether... [Pg.691]

C7H1GS HEXYL-METHYL- -137.588 5.7293E-01 1.1389E-04 43.47 365 C8H160 OCTYL- -361.386 7.9753E-01 6.3199E-05 -117.36... [Pg.380]

Substitutive lUPAC name l-(Methylthio)hexane Functional class name Hexyl methyl sulfide... [Pg.692]

Calcium hydride (CaH,) [7789-78-8], 12 Carbamic acid, (chlorosulfonyl)-, methyl ester [36914-92-8], 40 CARBAMIC ACID, HEXYL-, METHYL ESTER [22139-32-8],40 Carbamic acid, [2-oxo-2-[(phenylmethyl)-amino] ethyl], phenylmethyl ester [2642-32-2], 93... [Pg.133]

Carbamic acid, hexyl-, methyl ester, 40 CARBODIIMIDF, POLYMERIC [BENZENE, DIETHENYL-, POLYMER WITH ETHF.NYLBFNZFNE, [[[(<1-METHYLETHYL)IMINO ] METHYLENE] AMINO] METHYL] DERIV.],... [Pg.139]

Diazenecarboxylic acid, 2-(l-cyanocyclo-hexyl)-,methyl ester [33670-04-1], 58,102, 106... [Pg.128]

Hexyl methyl ketone, o36 Hexyl propyl ketone, d20 Hippuric acid, b70 Homocysteine, a200 Homopiperidine, h48 Homoveratric acid, d513 Homoveratrylamine, d517 Hydroacrylonitrile, hi 73 2-Hydrazinoethanol, hi 25... [Pg.237]

Hexyllithium, 15 147 Hexyl methyl carbonate molecular formula, 6 305t l-Hexyn-3-ol, l 249t 5-Hexynoic acid, 5 34t Hexynol... [Pg.432]

HEXYL-METHYL-SULFIDE 757.8673 -2.3337E+04 -3.0359E+02 2.6757E-01... [Pg.42]

HEPTANOL 5-HETHYL-l-HEXANOL ISOPROPYL-TERT-BUTYL-ETHER n-HEPTYL MERCAPTAN BUTYL-PROPYL-SULFIDE ETHYL-PENTYL-SULFIDE HEXYL-METHYL-SULFIDE... [Pg.69]

C7H16S HEXYL-METHYL-SULFIDE 6.046E-04 638.37 -0.7143 206.66 606.45 9.478E-04 0.839... [Pg.162]

Fig. 9 Decomposition mechanism of bis(hexyl(methyl)diselenocarbamato)zinc(II)... Fig. 9 Decomposition mechanism of bis(hexyl(methyl)diselenocarbamato)zinc(II)...
Benzyl-methyl-amtn Methyl- (2-phenyl-ethyl) -amin Cyclohexyl-methyl-amin Hexyl-methyl-amin... [Pg.707]

A022 CaHxeO hexyl methyl ketone 6vi CH3CO(CH2)5CHs EtOH at P0 KOH 1 - - - -/- 0-2 -... [Pg.356]

Hexyl methyl ketone, o34 Hexyl propyl ketone, dl6 Hippuric acid, b71 Histamine, i8 Homocysteine, a204 Homopiperidine, h51 Homoserines, al88, al89 Homoveratric acid, d447 Homoveratrylamine, d451... [Pg.263]

Cognate preparation. Hexyl methyl ketoxime. From hexyl methyl ketone (octan-2-one) (Expt 5.86) in 90 per cent yield b.p. 106-108 °C/12 mmHg. [Pg.776]

See other pages where Hexyl-methyl is mentioned: [Pg.225]    [Pg.225]    [Pg.225]    [Pg.598]    [Pg.478]    [Pg.42]    [Pg.40]    [Pg.867]    [Pg.16]    [Pg.188]    [Pg.187]    [Pg.259]    [Pg.993]    [Pg.205]    [Pg.478]    [Pg.632]    [Pg.667]    [Pg.609]    [Pg.1327]    [Pg.1336]   
See also in sourсe #XX -- [ Pg.707 , Pg.993 , Pg.1121 ]



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Hexyl

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