1825-68-9

Usage

Uses

Used in Organic Synthesis:
Dimethylmethoxychlorosilane is used as a silylating agent for [facilitating the conversion of certain functional groups in organic molecules] because of its ability to protect alcohols and phenols during reactions.
Used in Production of Organosilicon Compounds:
It is used as an intermediate in the production of other organosilicon compounds for [enabling the synthesis of a variety of organosilicon materials with diverse applications].
Used in Surface Coating Industry:
Dimethylmethoxychlorosilane is used as a hydrophobic and anti-corrosive coating for [providing surfaces with enhanced resistance to water, corrosion, and other environmental factors].
Used in Research and Development:
It is utilized in research and development for [exploring new applications and improving existing processes in various chemical and material science fields] due to its unique properties and reactivity.

InChI:InChI=1/C3H9ClOSi/c1-5-6(2,3)4/h1-3H3

Upstream product

• 57753-82-9 1-chloromethyl-hexahydro-azepin-2-one 
• 90101-24-9 methoxydimethylsilyl isothicyanate 
• 151237-85-3 methoxydimethylsilyl azide 
• 6840-02-4 N,N-dimethyl-P-phenylphosphonamidic chloride 
• 819-43-2 dibutyl chlorophosphate 
• 23272-12-0 methoxydimethylsilyl cyanide 
• 7719-12-2 phosphorus trichloride 
• 1112-39-6 dimethyldimethoxysilan 
• 75-78-5 dimethylsilicon dichloride 
• 676-83-5 methyldichlorophosphane 
• 67-56-1 methanol 

Downstream Products

• 17903-27-4 benzoyloxy-methoxy-dimethyl-silane 
• 5573-48-8 Bis--methyl-phosphin 
• 54747-90-9 Cumyl(methoxydimethylsilyl)peroxid 
• 32957-38-3 ethynylmethoxydimethylsilane 
• 58666-69-6 Dimethylmethoxy-(thiobenzyl)-silan 
• 18027-93-5 3.6-Bis-(methoxy-dimethyl-silyl)-cyclohexadien-(1.4) 
• 54731-56-5 dimethyl(cyclohexyl)methoxysilane 
• 17881-88-8 methoxydimethylphenylsilane 
• 111784-84-0 dimethyl(3-trifluoromethylphenyl)methoxysilane 
• 23761-74-2 dimethyl(2,3,4,5,6-pentafluorophenyl)methoxysilane 
• 67284-42-8 dimethyl(2-methoxyphenyl)methoxysilane 
• 62244-47-7 dimethyl(3-methylphenyl)methoxysilane 
• 51501-87-2 dimethyl(4-methylphenyl)methoxysilane 
• 138181-69-8 ((3S,4S,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-phenylsulfanyl-tetrahydro-pyran-3-yloxy)-methoxy-dimethyl-silane 

Relevant academic research and scientific papers

Production processes for triorganomonoalkoxysilanes and triorganomonochlorosilanes

A silane containing a bulky hydrocarbon group or groups R therein and having the formula (III) [in-line-formulae]R3-(x+y)(R1)x(R2)ySi(OR3) [/in-line-formulae] can be produced by reacting a silane of the formula (I) [in-line-formulae](R1)x(R2) ySiCl3-(x+y)(OR3) [/in-line-formulae] with a Grignard reagent of the formula (II) [in-line-formulae]RMgX [/in-line-formulae] Further, a tri-organo-chlorosilane of the formula (XIIa) [in-line-formulae](R1)(R2)(R3)SiCl [/in-line-formulae] can be produced by reacting a tri-organo-silane of the formula (XIa) [in-line-formulae](R1)(R2)(R3)SiZ1 [/in-line-formulae] with hydrochloric acid. Furthermore, a tri-organo-monoalkoxysilane of the formula (XXIII) [in-line-formulae]R3-(x+y)(R1)x(R2)ySi(OR3) [/in-line-formulae] can be produced when a silane of the formula (XXI) [in-line-formulae](R1)x(R2)ySiCl4-(x+y) [/in-line-formulae] is reacted with a Grignard reagent of the formula (XXII) [in-line-formulae]RMgX [/in-line-formulae] with addition of and reaction with an alcohol or an epoxy compound during the reaction.

ORGANOSILICON AND ORGANOPHOSPHORUS COMPOUNDS WITH PSEUDOHALIDE GROUPS. VI. SYNTHESIS OF ALKOXYDIMETHYLSILYL AZIDES AND SOME OF THEIR PROPERTIES

By reaction of sodium azide with alkoxydimethylsilyl chlorides in hexamethylphosphoramide previously unknown alkoxydimethylsilyl azides were prepared and some of their properties were studied.Silyl azides reacting with zinc difluoride, acyl halides, phosphorus acid chlorides, and perfluoro-2-aza-2-butene can replace halogen by both alkoxy and azido groups (depending on the nature of the halogen-containing compound).

ORGANOSILICON AND ORGANOPHOSPHORUS COMPOUNDS WITH PSEUDOHALIDE GROUPS. 2. REACTIONS OF ALKOXYDIMETHYLSILYL CYANIDES WITH CHLORIDES OF TRICOORDINATED PHOSPHORUS

Reactions of alkoxydimethylsilyl cyanides with some chlorides of tricoordinated phosphorus ("phosphorous chlorides") have been studied.It is shownd that, depending on the nature of the phosphorous chloride, the chlorine atoms can either be substituted onl