937-12-2

Basic information

• Product Name: Stannane, trimethyl(4-methylphenyl)-
• CAS NO: 937-12-2
• Molecular Formula: C10H16Sn
• Molecular Weight: 254.947
• Mol File: 937-12-2.mol
• Article Data: 29

Chemical Properties

• CAS DataBase Reference: Stannane, trimethyl(4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Stannane, trimethyl(4-methylphenyl)-(937-12-2)
• EPA Substance Registry System: Stannane, trimethyl(4-methylphenyl)-(937-12-2)

Safety Data

• Hazardous Substances Data: 937-12-2(Hazardous Substances Data)

Upstream product

• 106-38-7 para-bromotoluene 
• 1631-73-8 trimethylstannane 
• 4111-54-0 lithium diisopropyl amide 
• 1066-45-1 trimethyltin(IV)chloride 
• 13328-67-1 penta(p-tolyl)antimony(V) 
• 1066-44-0 trimethyltin bromide 
• 2417-95-0 p-tolyllithium 
• 661-69-8 hexamethyldistannane 
• 53188-52-6 1-(methylsulfonyl)-2-(4-methylphenyl)diazene 
• 106-49-0 p-toluidine 
• 624-31-7 4-tolyl iodide 
• 4294-57-9 para-methylphenylmagnesium bromide 
• 16507-95-2 triethyl(p-tolyl)tin 
• 17946-71-3 lithium trimethylstannyl 

Downstream Products

• 3333-13-9 p-allyltoluene 
• 811-73-4 trimethylstannyl iodide 
• 135741-04-7 methyl 3-<(benzyloxycarbonyl)amino>-2-(methoxycarbonyl)-5-oxo-5-(p-tolyl)pentanoate 
• 80-39-7 N-ethyl-4-methyl-benzenesulfonamide 
• 1066-45-1 trimethyltin(IV)chloride 
• 613-33-2 (4,4'-dimethyl-1,1'-biphenyl) 
• 5350-47-0 (4-methylphenyl)(4-nitrophenyl)methanone 
• 104-87-0 4-methyl-benzaldehyde 
• 114772-53-1 2-Cyano-4'-methylbiphenyl 
• 676-89-1 trimethyltin tetrafluoroborate 
• 46318-53-0 (CH₃)3SnOSOC₆H₄-p-CH₃ 
• 1247019-54-0 ethyl 1-cyclopropyl-6-fluoro-7-(4-methylphenyl)-8-nitro-4-oxo-1,4-dihydroquinoline-3-carboxylate 
• 352-32-9 p-fluorotoluene 
• 108-88-3 toluene 

Relevant articles and documents

Visible-Light-Driven Synthesis of Arylstannanes from Arylazo Sulfones

The visible-light-driven preparation of (hetero)aryl stannanes was carried out under both photocatalyst- and metal-free conditions via irradiation of arylazo sulfones in the presence of hexaalkyldistannanes. The reaction shows a high efficiency and a wide substrates scope. The resulting crude organotin derivatives can be directly employed in a Stille protocol.

NOVEL METHOD OF PREPARING BENZOIMIDAZOLE DERIVATIVES

This invention relates to a method of preparing a benzoimidazole derivative at high purity and high yield so as to enable the production of the benzoimidazole derivative compound as an antagonist against a vanilloid reactor-1, and particularly to a method

Rhodium-catalyzed boron arylation of 1,2-azaborines

A Sn-phony in B! BN isosteres of biphenyl compounds are prepared through Rh-catalyzed cross-coupling between 2-chloro-1,2-azaborines and arylstannanes (see scheme). The synthetic method should enable investigations of structure-activity relationships (SAR