18206-22-9

Basic information

• Product Name: Benzenamine, 2,2'-dithiobis[N,N-dimethyl-
• CAS NO: 18206-22-9
• Molecular Formula: C16H20N2S2
• Molecular Weight: 304.48
• Mol File: 18206-22-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenamine, 2,2'-dithiobis[N,N-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 2,2'-dithiobis[N,N-dimethyl-(18206-22-9)
• EPA Substance Registry System: Benzenamine, 2,2'-dithiobis[N,N-dimethyl-(18206-22-9)

Safety Data

• Hazardous Substances Data: 18206-22-9(Hazardous Substances Data)

Upstream product

• 1141-88-4 2-Aminophenyl disulfide 
• 74-88-4 methyl iodide 

Downstream Products

• 107647-26-7 sulfure de (dimethylamino-2) phenyle et de (methyl-3 buten-3 yn-1) yle 
• 74642-18-5 sulfure de n.butyle et d'o.dimethylamino-phenyle 
• 137935-62-7 methyl-4 phenyl-1 penten-4 yn-2 ol-1 
• 289487-10-1 1-[2-(N,N-Dimethylamino)phenylsulfinyl]cyclopentene 
• 642472-86-4 2-(N,N-dimethylamino)phenyl vinyl sulfoxide 

Relevant articles and documents

Asymmetric synthesis of 1-aryl and 1,3-diarylcyclopentenes by the Heck reaction of 1-sulfinylcyclopentenes with iodoarenes

The asymmetric synthesis of 1-aryl and 1,3-diarylcyclopentenes by Heck reaction of (R)-1-[o-(N,N-dimethylamino)phenylsufinyl]cyclopentene with iodoarenes is described. (C) 2000 Elsevier Science Ltd.

Asymmetric Intermolecular Pauson-Khand Reactions of Unstrained Olefins: The (o-Dimethylamino)phenylsulfinyl Group as an Efficient Chiral Auxiliary

The first asymmetric version of intermolecular Pauson?Khand reactions of unstrained alkenes is described. Generally simple acyclic alkenes exhibit low reactivity and regioselectivity in intermolecular Pauson?Khand reactions; however, o-(dimethylamino)phen