73639-62-0 Usage
Uses
Used in Organic Synthesis:
2,2-dimethyl-4-(chloromethyl)-1,3-dioxa-2-silacyclopentane is utilized as a reagent in organic synthesis for its ability to contribute to the formation of complex molecular structures. Its silicon and chlorine components facilitate specific chemical reactions that are essential in the synthesis of a range of organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,2-dimethyl-4-(chloromethyl)-1,3-dioxa-2-silacyclopentane serves as a precursor for the preparation of silicon-containing compounds. These compounds are integral in the development of new drugs and pharmaceutical agents, potentially enhancing the efficacy and properties of medications.
Used in Specialty Materials Production:
2,2-dimethyl-4-(chloromethyl)-1,3-dioxa-2-silacyclopentane is also used as a precursor in the production of specialty materials. Its unique silicon and chlorine composition allows for the creation of materials with specific properties that are tailored for use in various high-performance applications.
Safety and Environmental Considerations:
It is crucial to handle 2,2-dimethyl-4-(chloromethyl)-1,3-dioxa-2-silacyclopentane with care due to its potential health and environmental hazards. Proper management and safety measures are necessary to mitigate any risks associated with its use in chemical processes and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 73639-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,3 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73639-62:
(7*7)+(6*3)+(5*6)+(4*3)+(3*9)+(2*6)+(1*2)=150
150 % 10 = 0
So 73639-62-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H11ClO2Si/c1-9(2)7-4-5(3-6)8-9/h5H,3-4H2,1-2H3
73639-62-0Relevant academic research and scientific papers
Birkofer, Leonhard,Stuhl, Oskar
, p. 21 - 29 (1980)
Silylation of substituted dioles by means of hexamethyldisilazane leads to 2,2,7,7-tetramethyl-3,6-dioxa-2,7-disilaoctane derivatives.Reactions of these dioles with hexamethylcyclotrisilazane afford substituted 1,3-dioxa-2-silacyclopentanes.
