3292-88-4 Usage
Physical state
Colorless liquid
The compound appears as a colorless liquid, which means it does not have a distinct color and is in a liquid state at room temperature.
Boiling point
129-131°C
The compound boils and turns into vapor in the temperature range of 129-131°C.
Density
0.854 g/cm3
The density of the compound is 0.854 grams per cubic centimeter, which indicates its relative mass compared to water (with a density of 1 g/cm3).
Stability
Stable and non-reactive under normal conditions
The compound is considered stable and does not readily react with other substances under standard conditions, making it relatively safe to handle.
Usage
Building block in the production of organosilicon compounds
1-Oxa-2-silacyclopentane, 2,2-dimethylis commonly used as a starting material or building block for the synthesis of various other organosilicon compounds.
Applications
Industrial and research uses
The compound can be found in a variety of industrial and research applications, particularly in the field of organic synthesis and organosilicon chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 3292-88-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3292-88:
(6*3)+(5*2)+(4*9)+(3*2)+(2*8)+(1*8)=94
94 % 10 = 4
So 3292-88-4 is a valid CAS Registry Number.
3292-88-4Relevant articles and documents
Silicon tethered alkenyl transfer and Type I ene reactions
Robertson, Jeremy,O'Connor, Garry,Ringrose, Caroline L.,Middleton, Donald S.
, p. 8321 - 8333 (2007/10/03)
A range of vinyl silanes was prepared in order to investigate the possibility of effecting silicon tethered Type I ene cyclisations analogous to our previously reported Type II variant. Some of these substrates were found to undergo overall stereospecific alkenyl transfer via silacyclopentanol intermediates; in a homologous series, alkenyl transfer was accompanied by dehydration to provide 7-silylhepta-2,4-dienes in moderate yield. Formal Type I ene cyclisations were found to be successful for allysilane precursors resulting in the stereoselective formation of silacyclohexanols. (C) 2000 Elsevier Science Ltd.
