26697-68-7

Upstream product

• 3724-65-0 2-butenoic acid 
• 503-64-0 (Z)-but-2-enoic acid 
• 36297-22-0 (E)-2-bromo-2-butenoic acid 
• 5405-34-5 (Z)-2-bromobut-2-enoic acid 
• 600-30-6 erythro-2,3-dibromobutanoic acid 
• 50553-14-5 2,3-dibromo-butyraldehyde 
• 4786-20-3 crotononitrile 
• 107-93-7 (E)-but-2-enoic acid 
• 56-23-5 tetrachloromethane 
• 7726-95-6 bromine 
• 75-15-0 carbon disulfide 
• 10035-10-6 hydrogen bromide 
• 4021-75-4 rac-(2R,3S)-2,3-dibromobutan-1-ol 

Downstream Products

• 590-13-6 (Z)-1-propenyl bromide 
• 590-15-8 trans-2-propenyl bromide 
• 5469-24-9 methyl 2,3-dibromobutyrate 
• 600-30-6 (R,S/S,R)-α,β-dibromobutyric acid 
• 609-11-0 (+/-)-erythro-2,3-dibromo-butyric acid ethyl ester 
• 5350-86-7 anti-2,3-Diphenylbutanoic acid 
• 10035-10-6 hydrogen bromide 
• 3724-65-0 2-butenoic acid 
• 7553-56-2 iodine 
• 36297-22-0 (E)-2-bromo-2-butenoic acid 
• 590-14-7 1-bromo-1-propene 

Relevant academic research and scientific papers

Iodide-catalysed cyclization of unsaturated N-chloroamines: A new way to synthesise 3-chloropiperidines

Tetrabutylammonium iodide is a very efficient catalyst for the cyclization of unsaturated N-chloroamines. The catalysis seems to proceed through N-iodoamine intermediates, which act as a source of iodonium ions. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.