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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Silane, triethylmethoxy-

CC[Si](OC)(CC)CC Request for Quotation
Chemical Name: Silane, triethylmethoxy-
CAS Number: 2117-34-2
Product Number: AG00C17U(AGN-PC-0JSCJN)
Synonyms:
MDL No:
Molecular Formula: C7H18OSi
Molecular Weight: 146.3027

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Chemical Structure


Triethylmethoxysilane, also known as TMES, serves as a versatile reagent in chemical synthesis processes due to its unique properties. This organosilane compound is commonly utilized as a crosslinker or coupling agent in the production of various materials, such as silicone rubbers, adhesives, and coatings. In organic synthesis, Triethylmethoxysilane is frequently employed as a silylating agent, enabling the protection of reactive functional groups during multi-step reactions. Additionally, TMES can participate in hydrosilylation reactions, facilitating the introduction of silane groups into organic molecules to modify their physical and chemical properties. Its compatibility with a wide range of substrates and mild reaction conditions make Triethylmethoxysilane a valuable tool for synthetic chemists seeking efficient and controlled methods for functional group manipulation and material design.