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Allyl Sentence Examples

  • The simplest member of the series is acrolein, C 3 H 4 0 or CH 2: CH�CHO, which can be prepared by the oxidation of allyl alcohol, or by the abstraction of the elements of water from glycerin by heating it with anhydrous potassium bisulphate.
  • EUGENOL (allyl guaiacol, eugenic acid), C10H1202,anodoriferous principle; it is the chief constituent of oil of cloves, and occurs in many other essential oils.
  • Soc., 1901, 79, p. 828) has resolved benzyl-allyl-phenyl-methylamine iodide by boiling with silver d-camphorsulphonate in a nearly anhydrous mixture of acetone and ethyl acetate.
  • The residue crystallizes slowly, and the crystalline product is almost wholly d-benzyl-allyl-phenyl-ammonium-d-sulphonate, the corresponding /-compound remaining as a syrupy residue.
  • When heated with glycerin to ioo C. it yields formic acid and carbon dioxide; above this temperature, allyl alcohol is formed.
  • Allyl cyanide boils at 119° C. Benzonitrile boils at 190.6° C. When solidified it melts att7° C. It is easily soluble in alcohol and ether.
  • Allyl alcohol >>
  • Crotonic acid, so named from the fact that it was erroneously supposed to be a saponification product of croton oil, may be prepared by the oxidation of croton-aldehyde, CH3 CH:CH CHO, obtained by dehydrating aldol, or by treating acetylene successively with sulphuric acid and water; by boiling allyl cyanide with caustic potash; by the distillation of 0-oxybutyric acid; by heating paraldehyde with malonic acid and acetic acid to, oo C. (T.
  • Thiourea and many of its unsymmetrical derivatives have marked physiological action; thiourea causes a slowing of the pulse and respiration, cardiac failure, and death in convulsions; phenyl-, ethyland acetyl-thiourea are actively toxic. The most important derivative pharmacologically is allyl-thiourea, also known as thiosinamine or rhodallin, NH2 CS NH CH2 CH:CH2.
  • It may be synthetically prepared by distilling allyl ethylamine over heated lead oxide (W.
  • This substance when heated with hydriodic acid to 300° C. is converted into a-propyl piperidine, which can also be obtained by the reduction of a-allyl pyridine (formed from a-methyl pyridine and paraldehyde).
  • Drewson, Ber., 1883, 16, p. 2207); by passing the vapour of allyl aniline over heated lead oxide; by the condensation of ortho-aminobenzaldehyde with acetaldehyde in the presence of aqueous.
  • The following monatomic alcohols receive special treatment under their own headings: - Alcohol (Ethyl), Allyl Alcohol, Amyl Alcohols, Benzyl Alcohol, Butyl Acohols, Methyl Alcohol, and Propyl Alcohols.
  • ALLYL ALCOHOL, C 3 H 5 OH or CH 2 :CH�CH 2 OH, a compound which occurs in very small quantities in wood spirit.
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Also Mentioned In


  • quinalbarbitone
  • allylic
  • di-pimethane-rearrangement
  • diallyl
  • allyls
  • allylisothiocyanate
  • allylphosphine
  • allylsilane
  • allylphenol
  • allylborane

Words near allyl in the dictionary


  • ally
  • ally-pally
  • allyboration
  • allying
  • allyl
  • allyl alcohol
  • allyl-alcohol
  • allyl-chloride
  • allyl-isothiocyanate
  • allyl resin

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