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The reaction between phenylhydrazine and ω‐chloroacetophenone. (The reaction between ω‐halogenoketones and phenylhydrazine, V)

Jan Van Alphen

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Abstract

Abstract The compound obtained by Hess, the condensation product of phenylhydrazine and ω‐chloroacetophenone has been investigated and its properties can be explained by assigning to it the constitution 1: 3‐diphenyl‐(1: 2‐diazacyclobutene‐2). The structure of the compound obtained by Scholtz from phenylhydrazine and ω‐chloroacetophenone, has been elucidated and proved to be the bis‐phenylhydrazone of diphenacyl.

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What this paper is about

Abstract The compound obtained by Hess, the condensation product of phenylhydrazine and ω‐chloroacetophenone has been investigated and its properties can be explained by assigning to it the constitution 1: 3‐diphenyl‐(1: 2‐diazacyclobutene‐2). The structure of the compound obtained by Scholtz from phenylhydrazine and ω‐chloroacetophenone, has been elucidated and proved to be the bis‐phenylhydrazone of diphenacyl.

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Available abstract

Abstract The compound obtained by Hess, the condensation product of phenylhydrazine and ω‐chloroacetophenone has been investigated and its properties can be explained by assigning to it the constitution 1: 3‐diphenyl‐(1: 2‐diazacyclobutene‐2). The structure of the compound obtained by Scholtz from phenylhydrazine and ω‐chloroacetophenone, has been elucidated and proved to be the bis‐phenylhydrazone of diphenacyl.

Key concepts: Phenylhydrazine, Chemistry, Medicinal chemistry

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The reaction between phenylhydrazine and ω‐chloroacetophenone. (The reaction between ω‐halogenoketones and phenylhydrazine, V) — Research Paper | ScholarLens