1333204-10-6

Basic information

• Product Name: 2-((R)-1-(benzyloxy)octan-2-yl)benzo-1,3-dithiole
• Synonyms: 2-((R)-1-(benzyloxy)octan-2-yl)benzo-1,3-dithiole
• CAS NO: 1333204-10-6
• Molecular Weight: 372.596
• Mol File: 1333204-10-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-((R)-1-(benzyloxy)octan-2-yl)benzo-1,3-dithiole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-((R)-1-(benzyloxy)octan-2-yl)benzo-1,3-dithiole(1333204-10-6)
• EPA Substance Registry System: 2-((R)-1-(benzyloxy)octan-2-yl)benzo-1,3-dithiole(1333204-10-6)

Safety Data

• Hazardous Substances Data: 1333204-10-6(Hazardous Substances Data)

Upstream product

• 57842-27-0 1,3-benzodithiol-2-ylium tetrafluoroborate 
• 124-13-0 Octanal 
• 1333204-09-3 (R)-2-(benzo-1,3-dithiol-2-yl)octan-1-ol 
• 100-39-0 benzyl bromide 

Downstream Products

• 185517-21-9 (R)-(-)-arundic acid 
• 1333204-11-7 2-((R)-1-(benzyloxy)octan-2-yl)-2-ethylbenzo-1,3-dithiole 

Relevant articles and documents

A Versatile Organocatalytic Approach for the Synthesis of Enantioenriched gem-Difluorinated Compounds

The combination of a practical and highly enantioselective organocatalytic reaction, which allows the stereoselective introduction of a benzodithiol group, with a fluorination step, gives a new and effective strategy for the stereoselective synthesis of difluorinated building blocks. The benzodithiol group is a versatile and chameleonic group that can be further functionalized before fluorination, giving customized and tailored useful synthetic strategies. As an example of the application of this facile strategy, the effective enantioselective synthesis of difluoroarundic acid is described. All you need is fluor! The combination of a practical and highly enantioselective organocatalytic reaction with a fluorination step provides a new and effective strategy for the stereoselective synthesis of enantioenriched difluorinated building blocks (see scheme).