4142-85-2 Usage
Description
BIS(TRICHLOROSILYL)METHANE, with the chemical formula (Cl3Si)2CH2, is a colorless, odorless liquid that is highly flammable and reactive. It is a versatile chemical compound primarily used as a precursor in the production of silicon-containing materials and as an intermediate in the synthesis of other organosilicon compounds and organic chemistry reactions.
Uses
Used in Silicon-Containing Material Production:
BIS(TRICHLOROSILYL)METHANE is used as a precursor for the production of various silicon-containing materials, such as silicone rubber, resins, and coatings. Its reactivity allows for the formation of these materials with desired properties, making it an essential component in the manufacturing process.
Used in Organosilicon Compound Synthesis:
BIS(TRICHLOROSILYL)METHANE serves as an intermediate in the synthesis of other organosilicon compounds. Its unique structure and reactivity enable the creation of a wide range of organosilicon compounds with diverse applications in various industries.
Used in Organic Chemistry Reactions:
As a reagent in organic chemistry, BIS(TRICHLOROSILYL)METHANE is utilized in various reactions to facilitate the formation of desired products. Its reactivity and ability to form stable intermediates make it a valuable tool in the synthesis of complex organic molecules.
Used in Chemical Research and Development:
Due to its unique properties and reactivity, BIS(TRICHLOROSILYL)METHANE is also used in chemical research and development to explore new reactions, syntheses, and applications. Its potential in creating novel materials and compounds makes it an important compound in the field of chemical research.
Safety Precautions:
Given its reactivity and potential hazards, BIS(TRICHLOROSILYL)METHANE should be handled with caution and in accordance with proper safety protocols and regulations. This includes using appropriate personal protective equipment, working in well-ventilated areas, and following established guidelines for handling and storage of reactive chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 4142-85-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,4 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4142-85:
(6*4)+(5*1)+(4*4)+(3*2)+(2*8)+(1*5)=72
72 % 10 = 2
So 4142-85-2 is a valid CAS Registry Number.
InChI:InChI=1/CH2Cl6Si2/c2-8(3,4)1-9(5,6)7/h1H2
4142-85-2Relevant articles and documents
Process for Preparing Polysilylalkane
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Paragraph 0045-0047; 0056-0066; 0076-0078, (2020/04/17)
Polysilylalkane according to the present invention is represented by following formula. The present invention has an advantage that bis(silyl)alkanes or tri(silyl)alkanes can be manufactured in a high yield by dehydrochlorination with a small amount of catalyst by using a silane compound having a dichloro organic matter or a dichloromethyl group.COPYRIGHT KIPO 2020
Process for Preparing Polysilylalkane
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Paragraph 0056; 0058, (2016/11/02)
According to the present invention, polysilylalkane is represented by chemical formula 3. In chemical formula 3, m is equal to n, and n is equal to zero; and R^3 is a chloromethyl group. In the case of R^4 is H, -SiMe_2Cl, -SiMe_3, -SiMeCl_2, and -SiCl_3, R^3 is equal to -SiCl_3. In the case of R^4 is H, and R^5 is equal to R^6 and R^6 is equal to Me, or R^5 is equal to Me and R^6 is equal to Et, R^3 is -SiCl_3. In the case of R^4 is H, R^5 is equal to -CH_2SiCl_3, and R^6 is Me, R^3 is equal to -SiCl_3. In the case of R^4 is H, R^5 is equal to R^6 and R^6 is equal to -CH_2SiCl_3, R^3 is equal to Et, SiMe_2Cl, -SiMeCl_2, and -SiCl_3, and m is an integer of zero to nine. The manufacturing method is capable of manufacturing bis(silyl)alkane or tri(silyl)alkane in a high yield with a small amount of a catalyst.COPYRIGHT KIPO 2016
[2σ + 2σ + 2π]-Cycloaddition of quadricyclane to partially methylated chlorosilylalkenes
Chapala, Pavel P.,Bermeshev, Maxim V.,Lakhtin, Valentin G.,Genaev, Alexander M.,Tavtorkin, Alexander N.,Finkelshtein, Eugene Sh.
, p. 344 - 345 (2015/10/19)
[2σ + 2σ + 2π]-Cycloaddition of quadricyclane to trissilylated ethenes Cl3 - nMenSiCH=CSiMenCl3 - n(SiMe3 - nCln) (n = 1, 2) at 95 °C affords 3,3,4-trissilylated exo-tricyclo[4.2.1.02,5]non-7-enes. Tetrakis(trichlorosilyl)ethene does not react with quadricyclane.