3531-44-0

Usage

InChI:InChI=1/C2H5.3CH3.Sn/c1-2;;;;/h1H2,2H3;3*1H3;/rC5H14Sn/c1-5-6(2,3)4/h5H2,1-4H3

Upstream product

• 78-40-0 triethyl phosphate 
• 594-27-4 tetramethylstannane 
• 4282-05-7 dimethyl diethyl tin 
• 597-64-8 tetraethyltin 
• 1066-44-0 trimethyltin bromide 
• 132126-13-7 4,5,5-triethyl-2,5-dihydro-2,2-dimethyl-3-phenyl-1-(trimethylstannyl)-1,2,5-oxoniasilaboratole 
• 132126-09-1 4,5,5-triethyl-2,5-dihydro-2,3-dimethyl-2-phenyl-1-(trimethylstannyl)-1,2,5-oxoniasilaboratole 
• 1115-99-7 triethyl gallium 
• 1084-14-6 Me₃Sn(N(cyclohexyl)2) 

Downstream Products

• 80206-19-5 4-ethyl-[1,10]phenanthroline 
• 66-71-7 1,10-Phenanthroline 
• 31301-28-7 4-methyl-1,10-phenanthroline 
• 625-50-3 N-ethylacetamide 
• 507-19-7 t-butyl bromide 
• 74-88-4 methyl iodide 
• 594-27-4 tetramethylstannane 
• 1066-45-1 trimethyltin(IV)chloride 
• 108354-35-4 ethyl-dimethyl tin ⁽¹⁺⁾; dimethylethyl tin bromide 
• 1066-44-0 trimethyltin bromide 
• 35409-99-5 (CH₃)2Sn(C₂H₅)(CH(CH₃)C₆H₅) 
• 811-73-4 trimethylstannyl iodide 
• 75-03-6 ethyl iodide 

Relevant academic research and scientific papers

Synthesis of substituted aminogallanes by alkyltrimethyltin elimination

Alkyltrimethyltin elimination reactions of R3Ga (R = Me, Et) with R″R′NSnMe3 (R″ = i-Bu, SnMe3, C6H11 and R′ = i-Bu, i-Pr, C6H11) have been investigated. The aminogallanes [Mesu

Organosubstituted 2,5-Dihydro-1,2,5-oxoniasilaboratoles - Characterization and Reactivity

The potassium salt of the anions , prepared from the organosubstituted cis-2-boryl-1-silylalkenes 1a-d and KOH, react with the electrophiles R1Hal IV: ClElIV(CH3)3, ElIV = Si, Ge, Sn, Pb> to give the neutral five-membered ring compounds .On heating of 3H or 3Sn either ethyl migration occurs to yield the saturated diasteromers , or elimination of ethane takes place to give the unsaturated compounds .The reaction of 2 with ClPb(CH3)3 leads to 3Pb (11B-NMR), which exclusively form 5 with elimination of C2H5Pb(CH3)3.