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A solid S-methyl derivative (methyl 2-cyano-3- hydroxythiocrotonimidate) of the enol structure of ¢ô was obtained by treating ¢òwith methyl iodide in 4% sodium hydroxide  solution. The ethyl group of ¢ò was lost during this alkylation reaction.
      Upon mild oxidation of ¢ùwith iodine in potassium iodide, a disulfide, which was  characterized as 3,3'-dithiobis [2- (l-hydroxyethylidene)-3-imino propionitrile](¢ú¢ô), was formed.  It was surprising to find that if ¢ò was mildly oxidized in the same manner with iodine in potassium iodide the ethyl group was lost and the same product was formed. The absence of  hydrogen iodide salt formation was demonstrated by a negative halogen analysis.
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