68971-91-5

Basic information

• Product Name: Stannane, tributyl(2,4,6-trimethylphenyl)-
• CAS NO: 68971-91-5
• Molecular Formula: C21H38Sn
• Molecular Weight: 409.243
• Mol File: 68971-91-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Stannane, tributyl(2,4,6-trimethylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Stannane, tributyl(2,4,6-trimethylphenyl)-(68971-91-5)
• EPA Substance Registry System: Stannane, tributyl(2,4,6-trimethylphenyl)-(68971-91-5)

Safety Data

• Hazardous Substances Data: 68971-91-5(Hazardous Substances Data)

Upstream product

• 392-69-8 1-fluoro-2,4,6-trimethylbenzene 
• 17955-46-3 trimethylsilyltributyltin 
• 4028-63-1 iodomesitylene 
• 813-19-4 bis(tri-n-butyltin) 
• 4226-01-1 tri-n-butyltin lithium 
• 576-83-0 2,4,6-trimethylphenyl bromide 
• 1461-22-9 tributyltin chloride 
• 7342-47-4 tributyltin iodide 
• 159123-24-7 [Au(mesityl)(AsPh₃)] 
• 2633-66-1 2-mesitylmagnesium bromide 

Downstream Products

• 159123-24-7 [Au(mesityl)(AsPh₃)] 
• 581-80-6 4,4'-bis(trifluoromethyl)biphenyl 
• 98-08-8 α,α,α-trifluorotoluene 
• 66818-57-3 2,4,6-trimethyl-4'-(trifluoromethyl)-1,1'-biphenyl 
• 66818-60-8 ethyl 2',4',6'-trimethyl-[1,1'-biphenyl]-4-carboxylate 
• 954-16-5 2,4,6-Trimethylbenzophenon 
• 392-69-8 1-fluoro-2,4,6-trimethylbenzene 
• 22187-05-9 1-(2,4,6-trimethylphenyl)naphthalene 
• 973-78-4 2',4',6'-trimethyl-2,4-dinitroazobenzene 

Relevant articles and documents

Illuminating Stannylation

We have developed photoboosted stannylation reactions of terminal alkynes (linear-selective hydrostannylation) and fluoroarenes (defluorostannylation), in which the stannyl anion is photoexcited to an excited triplet (T1) stannyl diradical species. This u

Stannyl-Lithium: A Facile and Efficient Synthesis Facilitating Further Applications

We have developed a highly efficient, practical, polycyclic aromatic hydrocarbon (PAH)-catalyzed synthesis of stannyl lithium (Sn-Li), in which the tin resource (stannyl chloride or distannyl) is rapidly and quantitatively transformed into Sn-Li reagent at room temperature without formation of any (toxic) byproducts. The resulting Sn-Li reagent can be stored at ambient temperature for months and shows high reactivity toward various substrates, with quantitative atom efficiency.

FLUORINATION OF ORGANIC COMPOUNDS

Methods for fluorinating organic compounds are described herein.