80249-74-7 Usage
Uses
Used in Organic Chemistry:
Cyclopentylsilane is used as a versatile building block for the synthesis of various silicon-containing compounds, such as cyclopentylsilanols and cyclopentylsiloxanes. Its role in creating carbon-silicon bonds is pivotal in the development of new materials and pharmaceuticals.
Used in Material Science:
As a precursor, Cyclopentylsilane is instrumental in the production of silicon-based materials, which are essential in a variety of applications due to their unique properties.
Used in Pharmaceutical Development:
Cyclopentylsilane contributes to the advancement of pharmaceuticals by enabling the formation of carbon-silicon bonds, which are crucial in the synthesis of certain drug compounds.
Used in Specialty Silicones Production:
Cyclopentylsilane is used as a valuable intermediate in the manufacturing of specialty silicones, which are utilized in a wide array of industrial applications.
Used in Adhesive and Coating Industries:
CYCLOPENTYLSILANE is also employed in the production of adhesives and coatings, where its properties enhance the performance and characteristics of these products.
Check Digit Verification of cas no
The CAS Registry Mumber 80249-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,4 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 80249-74:
(7*8)+(6*0)+(5*2)+(4*4)+(3*9)+(2*7)+(1*4)=127
127 % 10 = 7
So 80249-74-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H12Si/c6-5-3-1-2-4-5/h5H,1-4H2,6H3
80249-74-7Relevant academic research and scientific papers
Reaction of Hydrogen Peroxide with Organosilanes under Chemical Vapour Deposition Conditions
Moore, Darren L.,Taylor, Mark P.,Timms, Peter L.
, p. 2673 - 2678 (2007/10/03)
When a stream of vapour at low pressure which contained a mixture of H2O2 with an organosilane, RSiH3 (R = alkyl or alkenyl), impinged on a silicon wafer, deposition of oxide films of nominal composition RxSiO(2-0.5x), where x 3 or higher alkenyl groups. or higher alkenylgroups. Possible mechanism for the Si-C bond cleavage reaction are discussed, with energetic rearrangement of radical intermediates of type Si(H)(R)(OOH)' being favoured.
Synthesis of Cyclobutyl- and Cyclopentylsilane
Dakkouri, Marwan,Kehrer, Hermann
, p. 3460 - 3461 (2007/10/02)
The reaction of iodosilane with cyclobutyl- or cyclopentylmagnesium bromide yielded cyclobutyl- (3) and cyclopentylsilane (4), respectively.Like cyclopropylsilane these new compounds show no reaction with oxygen or with water.
