1762-26-1

Usage

InChI:InChI=1/C2H5.3CH3.Pb/c1-2;;;;/h1H2,2H3;3*1H3;/rC5H14Pb/c1-5-6(2,3)4/h5H2,1-4H3

Upstream product

• 925-90-6 ethylmagnesium bromide 
• 1520-78-1 trimethyllead chloride 
• 74-87-3 methylene chloride 
• 75-00-3 chloroethane 
• 75-74-1 Tetramethylblei-(IV) 
• 78-00-2 tetraethyllead(IV) 
• 7446-70-0 aluminium trichloride 
• 6713-83-3 hexamethyldilead 
• 2388-00-3 hexaethyl diplumbane 
• 110-54-3 hexane 
• 1762-27-2 Diethyl-dimethyl-plumbane 
• 125878-71-9 potassium (2,4,5,5-tetraethyl-2,5-dihydro-2,3-dimethyl-1,2,5-oxasilaboratolate) 
• 125878-73-1 potassium (4,5,5-triethyl-2,5-dihydro-2,2-dimethyl-3-phenyl-1,2,5-oxasilaboratolate) 
• 125878-72-0 potassium (4,5,5-triethyl-2,5-dihydro-2,3-dimethyl-2-phenyl-1,2,5-oxasilaboratolate) 

Downstream Products

• 75-74-1 Tetramethylblei-(IV) 
• 1762-28-3 triethyl-methyl plumbane 
• 78-00-2 tetraethyllead(IV) 
• 17546-36-0 trimethyl lead ⁽¹⁺⁾; iodide 

Relevant academic research and scientific papers

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.