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Silane, trichloromethoxy-, also known as trichloro(methoxy)silane or chloromethyltrichlorosilane, is a colorless, volatile, and highly reactive liquid with the chemical formula Cl3SiCH3OCH3. It is a derivative of silane, where one hydrogen atom is replaced by a chloromethyl group and another by a methoxy group. Silane,trichloromethoxy- is primarily used as a coupling agent in the production of composite materials, particularly in the rubber and plastics industries, to improve adhesion between the inorganic and organic phases. It is also employed as a silylating agent in organic synthesis and as a precursor in the manufacture of other organosilicon compounds. Due to its reactivity, it is essential to handle trichloromethoxysilane with caution, as it can react violently with water and is highly corrosive.

1825-97-4

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1825-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1825-97-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1825-97:
(6*1)+(5*8)+(4*2)+(3*5)+(2*9)+(1*7)=94
94 % 10 = 4
So 1825-97-4 is a valid CAS Registry Number.

1825-97-4Relevant academic research and scientific papers

PROCESS FOR SELECTIVE PRODUCTION OF HALOSILANES FROM SILICON-CONTAINING TERNARY INTERMETALLIC COMPOUNDS

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Paragraph 0041, (2014/08/06)

A process includes contacting an organohalide with a ternary intermetallic compound at a temperature of 300 °C to 700 °C to form a reaction product including a halosilane. The ternary intermetallic compound includes three metals. The first metal is Cu or Mg; the second metal is Au, Ni, or Pd; and the third metal is Si.

ALTERNATIVE METHODS FOR THE SYNTHESIS OF ORGANOSILICON COMPOUND

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Paragraph 0053-0055, (2013/09/26)

A method of forming chloro-substituted silanes from the reaction of an alkoxysilane with a chlorinating agent in the optional presence of a catalyst is provided. More specifically, chloro-substituted silanes, including but not limited to silicon tetrachloride, are formed by reacting a chlorinating agent, such as thionyl chloride, with an alkylalkoxysilane having the formula (R'0)4-xSiRx, where R and R' are independently selected alkyl groups comprising one or more carbon atoms and x is 0, 1, 2, or 3. The catalyst may be dimethylformamide, (chloromethylene)dimethyliminium chloride, or triethylamine, among others. The chloro- substituted silane formed in the reaction along with several by-products has the formula (RO)4-x-ySiRxCly; where x is 0, 1, 2, or 3 and y is 1, 2, 3, or 4. One of the by-products of the reaction is an alkyl chloride.

Alternative methods for the synthesis of organosilicon compounds

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Paragraph 0029; 0059-0061, (2013/09/26)

A method of forming chloro-substituted silanes from the reaction of an alkoxy-or acetoxy-substituted silane with a chlorinating agent in the optional presence of a catalyst is provided. For instance, chloro-substituted silanes, including but not limited to silicon tetrachloride, are formed by reacting a chlorinating agent, such as thionyl chloride, with an alkoxysilane having the formula (R'O)4-xSiRx, where R and R' are independently selected alkyl groups comprising one or more carbon atoms and x is 0, 1, 2, or 3. The catalyst may be dimethylformamide, (chloromethylene)dimethyliminium chloride, or triethylamine, among others. The chloro-substituted silane formed in the reaction along with several by-products has the formula (R'O)4-x-ySiRxCly; where x is 0, 1, 2, or 3 and y is 1, 2, 3, or 4. One of the by-products of the reaction is an alkyl chloride.

Formation of organo-inorganic hybrid networks in the system consisting of Tris(2,2-bipyridine)ruthenium complexes and silica

Zdravkov,Aleksandrova,Aseev,Nikonorov,Khimich

scheme or table, p. 1532 - 1537 (2009/05/06)

Organo-inorganic composites consisting of mutually linked ruthenium complexes with organic ligands and an inorganic SiO2 network were synthesized by the sol-gel method. The luminescence and photosensitive properties of the resulting compounds w

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