20473-36-3

Upstream product

• 104-55-2 3-phenyl-propenal 
• 14371-10-9 (E)-3-phenylpropenal 
• 67-66-3 chloroform 
• 7782-50-5 chlorine 

Downstream Products

• 18365-42-9 α-chloro-cinnamaldehyde 
• 99414-74-1 α-chlorocinnamaldehyde 
• 122195-83-9 α-chloro-2-nitro-cinnamic acid 
• 851282-97-8 (Z)-2-chloro-3-(2-nitrophenyl)acrylaldehyde 
• 35088-92-7 α-chloro-cis-cinnamaldehyde seqtrans-oxime 
• 60951-73-7 α-chloro-4-nitro-cinnamic acid 
• 3626-97-9 2-chloro-3-(4-nitro-phenyl)-propenal 
• 705-54-4 (Z)-α-chlorocinnamic acid 
• 33603-89-3 (Z)-2-chloro-3-phenyl-2-propenal 
• 35115-76-5 2,3-dichloro-3-phenyl-propionic acid 

Relevant academic research and scientific papers

A convenient halogenation of α,β-unsaturated carbonyl compounds with OXONE and hydrohalic acid (HBr,HCl)

Mixtures of OXONE and hydrobromic acid or hydrochloric acid afford solutions of bromine or chlorine, respectively, α-Bromo- or α-chloro-α,β-unsaturated carbonyl compounds were prepared by addition of hydrobromic acid or hydrochloric acid to the mixture of

Oxidation of α,β-enones and alkenes with oxone and sodium halides: A convenient laboratory preparation of chlorine and bromine

Mixtures of oxone and sodium chloride or sodium bromide afford solutions of chlorine or bromine, respectively. These solutions effectively add chlorine and bromine to α,β-enones and alkenes. The method affords improved yields of 3-alkyl-2-halo-2-cycloalkenones which are sometimes difficult to prepare.