3937-30-2 Usage
Uses
Used in Organic Synthesis:
Allyldimethylsilane is used as a reagent for the production of various silicon-containing compounds, contributing to the synthesis of organic compounds with unique properties.
Used in Pharmaceutical Industry:
In the pharmaceutical field, allyldimethylsilane is used as a basic starting material for the development of functionalized silane derivatives, which have potential applications in drug discovery and development.
Used in Agrochemical Industry:
Similarly, in agrochemicals, allyldimethylsilane is utilized to create functionalized silane derivatives that can be employed in the formulation of pesticides, herbicides, and other agricultural chemicals.
Used in Materials Science:
In the realm of materials science, allyldimethylsilane is used as a component in the synthesis of advanced materials, including those with unique mechanical, electrical, or optical properties.
Used as an Allylating Agent:
Allyldimethylsilane is also used as an important allylating agent in the synthesis of organic compounds, due to its excellent compatibility with various catalytic systems, which facilitates the formation of allyl-containing products.
Check Digit Verification of cas no
The CAS Registry Mumber 3937-30-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,3 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3937-30:
(6*3)+(5*9)+(4*3)+(3*7)+(2*3)+(1*0)=102
102 % 10 = 2
So 3937-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H12Si/c1-4-5-6(2)3/h4,6H,1,5H2,2-3H3
3937-30-2Relevant academic research and scientific papers
Stationary and Pulsed Photolysis and Pyrolysis of 1,1-Dimethylsilacyclobutane
Brix, Th.,Arthur, N. L.,Potzinger, P.
, p. 8193 - 8197 (2007/10/02)
A study of the photolysis of 1,1-dimethylsilacyclobutane at 147 - 214 nm shows that of the four primary processes identified the predominant mode of decomposition is to C2H4 and dimethylsilaethene.Evidence from experiments in the presence of SF6 suggests that the dimethylsilaethene is formed initially in a vibrationally excited state: +hν -> Me2SiCH2v + CH2=CH2.Laser pulsed photolysis experiments at 193 nm have been carried out to measure tha absorption spectrum of Me2SiCH2, its absorption cross section, and the rate constant for Me2SCH2 combination: 2Me2SiCH2 -> (Me2SiCH2)2.The values obtained are ? (240 nm, base e) = (1.0 +/- 0.2)E-17 cm2 and k7 = (3.3 +/- 0.8)E-11 cm3 s-1.The kinetics of the pyrolysis of have also been reexamined, yielding the following rate constant expressions: k1/(s-1) = E(15.46 +/- 0.13) exp(-(31043 +/- 218)/T) and k-1/k71/2/(cm3/2s-1/2) = E(-7.0 +/- 0.3) exp(-(7850 +/- 300)/T).From these results, the heat of formation, ?-bond energy, and entropy of Me2SiCH2, have been deduced: ΔHfθ (g, 298 K) = 36 +/- 7 kJ mol-1, B? = 157 +/- 11 kJ mol-1, and Sθ(g, 298 K) = 332 +/- 8 J mol-1 K-1.
