1308304-50-8

Basic information

• Product Name: 1-(4-(4-iodo-3-methoxy-3-methylbutoxy)butoxy)-4-methylbenzene
• Synonyms: 1-(4-(4-iodo-3-methoxy-3-methylbutoxy)butoxy)-4-methylbenzene
• CAS NO: 1308304-50-8
• Molecular Weight: 406.304
• Mol File: 1308304-50-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(4-(4-iodo-3-methoxy-3-methylbutoxy)butoxy)-4-methylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-(4-iodo-3-methoxy-3-methylbutoxy)butoxy)-4-methylbenzene(1308304-50-8)
• EPA Substance Registry System: 1-(4-(4-iodo-3-methoxy-3-methylbutoxy)butoxy)-4-methylbenzene(1308304-50-8)

Safety Data

• Hazardous Substances Data: 1308304-50-8(Hazardous Substances Data)

Upstream product

• 3257-49-6 4-bromo-1-(4'-methylphenoxy)butane 
• 106-44-5 p-cresol 
• 67-56-1 methanol 
• 1308304-54-2 1-methyl-4-(4-((3-methylbut-3-en-1-yl)oxy)butoxy)benzene 

Downstream Products

• 1308304-60-0 1-(4-(3-methoxy-3-methylbutoxy)butoxy)-4-methylbenzene 
• 60222-64-2 4-(p-tolyloxy)butan-1-ol 

Relevant articles and documents

Fragmentations observed in the reactions of α-methoxy-γ- alkoxyalkyl iodide substrates with super-electron-donors derived from 4-DMAP and N-methylbenzimidazole

Reactions of super-electron-donors (SEDs) derived from 4- dimethylaminopyridine and from N-methylbenzimidazole with α-methoxy- γ-alkoxyalkyl iodides lead to liberation of the γ-alkoxy groups as their alcohols. This is consistent with generation of alkyl radicals from the alkyl halide precursors, and trapping of these radicals by the radical-cation of the SED, followed by a heterolytic fragmentation.