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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, [(1-ethoxy-2-methyl-1-propenyl)oxy]trimethyl-

CCOC(=C(C)C)O[Si](C)(C)C Request for Quotation
Chemical Name: Silane, [(1-ethoxy-2-methyl-1-propenyl)oxy]trimethyl-
CAS Number: 31469-16-6
Product Number: AG0032AN(AGN-PC-0NDM6Q)
Synonyms:
MDL No:
Molecular Formula: C9H20O2Si
Molecular Weight: 188.3394

Identification/Properties

Properties
BP:
182.377°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
188.342g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
188.123g/mol
Monoisotopic Mass:
188.123g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
12
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Ethoxy-2-methyl-1-(trimethylsiloxy)-1-propene is a versatile compound used extensively in chemical synthesis due to its unique reactivity and functional groups. This compound serves as a valuable building block in the creation of various organic compounds through its ability to participate in a range of essential chemical reactions.In chemical synthesis, 1-Ethoxy-2-methyl-1-(trimethylsiloxy)-1-propene can be employed as a key intermediate in the synthesis of complex molecules such as pharmaceuticals, agrochemicals, and specialty chemicals. Its trimethylsiloxy group can serve as a protecting group for alcohols, enabling selective transformations in the presence of other functional groups. Additionally, the ethoxy and methyl groups provide opportunities for further elaboration through various chemical manipulations.Furthermore, the propene moiety in this compound offers the potential for participation in important reactions such as hydroboration, addition reactions, and cross-coupling reactions, allowing for the introduction of diverse functional groups with high stereocontrol. Overall, the versatile nature of 1-Ethoxy-2-methyl-1-(trimethylsiloxy)-1-propene makes it a valuable tool for synthetic chemists seeking to access structurally complex and biologically relevant compounds.