1612786-69-2

Basic information

• Product Name: ethyl(phenyl(2,4,6-trimethoxyphenyl)methyl)sulfane
• Synonyms: ethyl(phenyl(2,4,6-trimethoxyphenyl)methyl)sulfane
• CAS NO: 1612786-69-2
• Molecular Weight: 318.437
• Mol File: 1612786-69-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl(phenyl(2,4,6-trimethoxyphenyl)methyl)sulfane(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl(phenyl(2,4,6-trimethoxyphenyl)methyl)sulfane(1612786-69-2)
• EPA Substance Registry System: ethyl(phenyl(2,4,6-trimethoxyphenyl)methyl)sulfane(1612786-69-2)

Safety Data

• Hazardous Substances Data: 1612786-69-2(Hazardous Substances Data)

Upstream product

• 621-23-8 1,2,3-trimethoxybenzene 
• 100-52-7 benzaldehyde 
• 75-08-1 ethanethiol 
• 1323902-49-3 tert-butyl ((ethylthio)(phenyl)methyl)carbamate 

Downstream Products

• 621-23-8 1,2,3-trimethoxybenzene 
• 7334-52-3 benzaldehyde diethyldithioacetal 
• 22807-99-4 1,3,5-trimethoxy-2-(phenylmethyl)benzene 

Relevant articles and documents

INTRODUCTION OF ALKYL SUBSTITUENTS TO AROMATIC COMPOUNDS

Novel selective synthesis route to introduce primary alkyl groups on aromatic compounds is disclosed. The synthesis route is based on electrophilic aromatic substitutions of thionium ion species that are generated in-situ from aldehydes and thiols, affording benzyl sulfide that can be reduced with triethylsilane.

NIS-assisted aza-Friedel-Crafts reaction with α-carbamoysulfides as precursors of N-carbamoylimines

A general and practical N-iodosuccinimide (NIS)-promoted aza-Friedel-Crafts reaction of various aromatic nucleophiles with N-acylimines generated in situ from α-amidosulfides to give a rapid access to highly functionalized amines is described. The newly developed methodology is very mild, fast, efficient, and complementary.