3944-18-1 Usage
Uses
Used in Chemical Industry:
Vinylmethylsilacyclopentane is used as a chemical building block for the synthesis of silicon-containing polymers and materials, due to its thermal stability and the ability to modify its properties through functionalization.
Used in Organosilicon Chemistry:
In the field of organosilicon chemistry, vinylmethylsilacyclopentane is utilized as a precursor for the synthesis of complex organic molecules, highlighting its role in creating advanced materials and compounds.
Used in Material Science:
VINYLMETHYLSILACYCLOPENTANE is employed in material science for the development of new materials with enhanced properties, leveraging its thermal stability and reactivity in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 3944-18-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,4 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3944-18:
(6*3)+(5*9)+(4*4)+(3*4)+(2*1)+(1*8)=101
101 % 10 = 1
So 3944-18-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H14Si/c1-3-8(2)6-4-5-7-8/h3H,1,4-7H2,2H3
3944-18-1Relevant academic research and scientific papers
SYNTHETIC PROCESS FOR CYCLIC ORGANOSILANES
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Page/Page column 10-11, (2008/06/13)
A process for preparing a cyclic organosilane using a solvent that promotes ring-closure reactions between an organosilane compound and a dihalo organic compound is disclosed. The ring-closure reactions may form a 4-, 5- or 6-member cyclic organosilane. The process involves a mixture including a dihalo organic compound, an organosilane having at least two functional groups, a solvent and magnesium (Mg). The two functional groups in the organosilane may include halogen, alkoxy or a combination thereof. In the presence of Mg, a Grignard intermediate is formed from the dihalo organic compound in the mixture. The solvent favors intra-molecular or self-coupling reactions of the Grignard intermediate. The intra-molecular or self-coupling reaction promotes ring-closure reaction of the Grignard intermediate to form the cyclic organosilane.
