Aliphatic Halogenation

Table 111,42 deals with a number of aliphatic halogen compounds together with their crystalline derivatives. Some aromatic compounds, which simulate the properties of aliphatic haUdes in some respects, are included. [Pg.292]

Aliphatic Halogen Compounds, Table III, 42 Aromatic Halogen Compounds, Table IV, 28. Aliphatic Ethers, Table III, 60. [Pg.1082]

In addition to its water solubility poly(vinyl pyrrolidone) is soluble in a very wide range of materials, including aliphatic halogenated hydrocarbons (methylene dichloride, chloroform), many monohydric and polyhdric alcohols (methanol, ethanol, ethylene glycol), some ketones (acetyl acetone) and lactones (a-butyrolactone), lower aliphatic acids (glacial acetic acid) and the nitro-paraffins. The polymer is also compatible with a wide range of other synthetic polymers, with gums and with plasticisers. [Pg.475]

The alkali salts of thiophenethiols react normally with aliphatic halogen compounds to give and have also been... [Pg.87]

It is only in relatively recent years that the interaction of indole Grignard reagents with unsaturated aliphatic halogen compounds has... [Pg.51]

B. Sample Mass Spectrum of an Aliphatic Halogenated Compound... [Pg.82]

Heating the Tube.—Place the iron case with its tube in a bomb or tube furnace in such a way that the end with the capillary is raised somewhat and directed towards the wall on which a shield is fixed and close the furnace. Several tubes may be heated simultaneously. Light all the burners and heat gradually to the desired temperature, regulating the gas supply at the main tap. For aliphatic halogen compounds (and many sulphur compounds) this temperature is about 250°, for the aromatic compounds (and sul-phonic acids) it is about 300°. Most substances are completely oxidised after three to four hours, but in the case of aromatic compounds the heating is continued for some hours longer. [Pg.71]

McLafferty, F.W. Mass Spectrometric Analysis. 1. Aliphatic Halogenated Compounds. Anal. Chem. 1962,34,2-15. [Pg.321]

Kramers, P.G., Mout, H.C., Bissumbhar, B. Mulder, C.R. (1991) Inhalation exposure in Drosophila mutagenesis assays experiments with aliphatic halogenated hydrocarbons, with emphasis on the genetic activity profile of 1,2-dichloroethane. Mutat. Res., 252, 17-33... [Pg.306]

Devotta, S., and V. R. Pendyala, Modified Joback Group Contribution Method for Normal Boiling Point of Aliphatic Halogenated Compounds. Ind. Eng. Chem. Res., 1992 31, 2042-2046. [Pg.107]

Reaction XXXVUI. (a) Action of Aqueous and Alcoholic Potassium or Sodium Cyanide on Aliphatic Halogen Compounds, and Hydrolysis of the Nitriles so formed. (B., 14, 1965 15, 2318.)—The preparation and hydrolysis of nitriles are dealt with on p. 151 and p. 239 respectively. In many cases, however, it is unnecessary to isolate the nitrile it can be directly hydrolysed to the corresponding acid on its formation. Among others, the following syntheses have been carried out in this way — i (i.) w-Valeric acid [jpentan acid] from w-butyl bromide (Am. Soc., 42, 310). [Pg.124]

Reaction CXXXII. Action of Aliphatic Halogen Compounds on Aliphatic or Aromatic Primary Amines.—Secondary, tertiary and quaternary compounds may be formed. [Pg.293]

The brain uptake efficiency and distribution of the above compounds as well as D2 receptor affinities of derivatives of spiperone containing aliphatic halogens have been studied also330. [Pg.1004]

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