146404-40-2

Basic information

• Product Name: 1-tosyl-1-hexadecylhydrazine
• Synonyms: 1-tosyl-1-hexadecylhydrazine
• CAS NO: 146404-40-2
• Molecular Weight: 410.665
• Mol File: 146404-40-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-tosyl-1-hexadecylhydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-tosyl-1-hexadecylhydrazine(146404-40-2)
• EPA Substance Registry System: 1-tosyl-1-hexadecylhydrazine(146404-40-2)

Safety Data

• Hazardous Substances Data: 146404-40-2(Hazardous Substances Data)

Upstream product

• 18049-99-5 N-hexadecyl-p-toluenesulfonamide 
• 159690-31-0 1-p-Toluolsulfonyl-1-phenethyl-hydrazin 
• 151259-26-6 C₁₉H₃₄N₂O₂S 
• 98-59-9 p-toluenesulfonyl chloride 
• 146404-41-3 C₁₅H₁₇ClN₂O₂S 
• 141666-87-7 1-Tosyl-1-<2-(4-methoxyphenyl)ethyl>hydrazine 
• 141666-92-4 4-methyl-N-[2-(4-methoxyphenyl)ethyl]benzenesulfonamide 
• 141666-91-3 N-[2-(4-chlorophenyl)ethyl]-4-methylbenzenesulfonamide 
• 1635-09-2 N-dodecyl-4-methylbenzenesulfonamide 
• 5450-75-9 4-methyl-N-(2-phenylethyl)benzenesulfonamide 
• 143-27-1 hexadecylamine 
• 536-57-2 p-toluene sulfinic acid 

Downstream Products

• 5450-75-9 4-methyl-N-(2-phenylethyl)benzenesulfonamide 
• 1635-09-2 N-dodecyl-4-methylbenzenesulfonamide 
• 1950-69-2 toluene-p-sulfonyl bromide 
• 141666-91-3 N-[2-(4-chlorophenyl)ethyl]-4-methylbenzenesulfonamide 
• 141666-92-4 4-methyl-N-[2-(4-methoxyphenyl)ethyl]benzenesulfonamide 
• 141666-87-7 1-Tosyl-1-<2-(4-methoxyphenyl)ethyl>hydrazine 
• 146404-41-3 C₁₅H₁₇ClN₂O₂S 
• 151259-26-6 C₁₉H₃₄N₂O₂S 
• 159690-31-0 1-p-Toluolsulfonyl-1-phenethyl-hydrazin 
• 112-82-3 hexadecanyl bromide 
• 4860-03-1 1-Chlorohexadecan 
• 98-59-9 p-toluenesulfonyl chloride 
• 36653-82-4 1-Hexadecanol 
• 544-76-3 Hexadecane 

Relevant articles and documents

A Convenient Conversion of Primary Amines into the Corresponding Halides Radical Promoted Halodeamination via N-Substituted-N-Tosylhydrazines

Treatment of 1-substituted-1-tosylhydrazines with 2 equivalents of NCS or NBS in dry THF in presence of light affords the corresponding alkyl halides in good yields.This reaction presumably involves the initial formation of a stabilized hydrazyl radical which is halogenated in a radical chain process.Elimination of p-toluenesulfinic acid and extrusion of nitrogen leads to the corresponding alkyl halide.This route provides an improved method for halodeamination under neutral reaction conditions.