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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, ethenyltris(1-methylethoxy)-

C=C[Si](OC(C)C)(OC(C)C)OC(C)C Request for Quotation
Chemical Name: Silane, ethenyltris(1-methylethoxy)-
CAS Number: 18023-33-1
Product Number: AG0021TI(AGN-PC-0JLWRV)
Synonyms:
MDL No:
Molecular Formula: C11H24O3Si
Molecular Weight: 232.3920

Identification/Properties

Computed Properties
Molecular Weight:
232.395g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
7
Exact Mass:
232.149g/mol
Monoisotopic Mass:
232.149g/mol
Topological Polar Surface Area:
27.7A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
164
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
1993
Hazard Statements:
H226
Precautionary Statements:
P210-P403+P235
Class:
3
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Triisopropoxy(vinyl)silane is a versatile chemical compound commonly used in chemical synthesis for various applications. In organic synthesis, it serves as a crucial reagent for the functionalization of organic molecules containing vinyl groups. By acting as a source of reactive vinyl functionality, Triisopropoxy(vinyl)silane enables the introduction of vinylsilane moieties into target molecules, facilitating further derivatization and modification through diverse downstream reactions. This compound significantly enhances the synthetic accessibility of complex organic molecules by providing a flexible strategy for the selective and efficient installation of vinyl groups, thereby enabling the creation of novel functional materials and pharmaceutical intermediates. Furthermore, Triisopropoxy(vinyl)silane plays a vital role in cross-coupling reactions, polymerization processes, and surface modification techniques, showcasing its remarkable utility in modern chemical synthesis methodologies.