132126-10-4

Basic information

• Product Name: 4,5,5-triethyl-2,5-dihydro-2,2-dimethyl-3-phenyl-1,2,5-oxoniasilaboratole
• CAS NO: 132126-10-4
• Molecular Weight: 274.286
• Mol File: 132126-10-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4,5,5-triethyl-2,5-dihydro-2,2-dimethyl-3-phenyl-1,2,5-oxoniasilaboratole(CAS DataBase Reference)
• NIST Chemistry Reference: 4,5,5-triethyl-2,5-dihydro-2,2-dimethyl-3-phenyl-1,2,5-oxoniasilaboratole(132126-10-4)
• EPA Substance Registry System: 4,5,5-triethyl-2,5-dihydro-2,2-dimethyl-3-phenyl-1,2,5-oxoniasilaboratole(132126-10-4)

Safety Data

• Hazardous Substances Data: 132126-10-4(Hazardous Substances Data)

Upstream product

• 593-81-7 trimethylamine hydrochloride 
• 125878-73-1 potassium (4,5,5-triethyl-2,5-dihydro-2,2-dimethyl-3-phenyl-1,2,5-oxasilaboratolate) 

Downstream Products

• 132020-99-6 4,5-diethyl-2,5-dihydro-2,2-dimethyl-3-phenyl-1,2,5-oxasilaborole 
• 132125-73-6 rac-4,4,5-triethyl-2,2-dimethyl-3-phenyl-1,2,5-oxasilaborolane 
• 4426-31-7 diethylboric acid 

Relevant articles and documents

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.