41159-04-0

Basic information

• Product Name: 2-(2,4,6-trimethylphenyl)-1,3-dithiolane
• CAS NO: 41159-04-0
• Molecular Formula: C₁₂H₁₆S₂
• Molecular Weight: 224.3854
• Mol File: 41159-04-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 359.6°C at 760 mmHg
• Flash Point: 175.2°C
• Density: 1.118g/cm³
• Vapor Pressure: 4.86E-05mmHg at 25°C
• Refractive Index: 1.604
• CAS DataBase Reference: 2-(2,4,6-trimethylphenyl)-1,3-dithiolane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,4,6-trimethylphenyl)-1,3-dithiolane(41159-04-0)
• EPA Substance Registry System: 2-(2,4,6-trimethylphenyl)-1,3-dithiolane(41159-04-0)

Safety Data

• Hazardous Substances Data: 41159-04-0(Hazardous Substances Data)

Upstream product

• 487-68-3 mesytaldehyde 
• 540-63-6 ethane-1,2-dithiol 
• 36896-65-8 bis(dimethylaluminium) 1,2-ethanedithiolate 

Downstream Products

• 103383-72-8 1-(difluoromethyl)-2,4,6-trimethylbenzene 

Relevant articles and documents

Concise total syntheses of palominol, dolabellatrienone, β-araneosene, and isoedunol via an enantioselective Diels-Alder macrobicyclization

Concise total syntheses of four members of the dolabellane family of diterpenoid natural products are reported. Key features of the developed route include the first demonstration of an enantioselective, intramolecular Type I Diels-Alder macrobicyclization, the first example of a stereoselective π-allyl Stille coupling reaction involving a farnesyl-derived intermediate, a powerful new reagent for the formation of dithianes with acid-sensitive molecules, and a unique and highly efficient ring-contraction sequence based on a modified Wolff photochemical rearrangement. Copyright

Comparative radioprotective activity of various pentagonal compounds with two heteroatomes

Various heterocyclic compounds with two heteroatomes were synthesized and their potential radioprotective activity was tested. This study shows the interest of phenylthiazolidines derivatives in chemical radioprotection.