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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, trimethyl-1-pentynyl-

CCCC#C[Si](C)(C)C Request for Quotation
Chemical Name: Silane, trimethyl-1-pentynyl-
CAS Number: 18270-17-2
Product Number: AG00243D(AGN-PC-0KKO94)
Synonyms:
MDL No:
Molecular Formula: C8H16Si
Molecular Weight: 140.2981

Identification/Properties

Properties
Storage:
Room Temperature;Inert atmosphere;
Form:
Liquid
Computed Properties
Molecular Weight:
140.301g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
140.102g/mol
Monoisotopic Mass:
140.102g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
128
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


Trimethyl(pent-1-yn-1-yl)silane is a versatile compound that finds wide application in chemical synthesis, particularly in the field of organosilicon chemistry. This compound serves as a valuable building block in the production of various silicon-containing materials and specialty chemicals. Notably, the presence of both alkynyl and trimethylsilyl groups in its structure imparts unique reactivity and functionality to trimethyl(pent-1-yn-1-yl)silane, making it a valuable tool in organic synthesis.In chemical synthesis, trimethyl(pent-1-yn-1-yl)silane can be used as a key intermediate in the preparation of functionalized organosilanes and silicones. Its alkynyl functionality allows for facile transformations via various metal-catalyzed coupling reactions, such as Sonogashira or Glaser couplings, enabling the introduction of diverse functional groups onto the silicon atom. Additionally, the trimethylsilyl group can serve as a protecting group for sensitive functional moieties during synthetic transformations.Furthermore, the unique properties of trimethyl(pent-1-yn-1-yl)silane make it a valuable reagent in the preparation of organosilicon polymers and materials with tailored properties. By incorporating this compound into polymerization reactions, researchers can introduce silicon-containing units into the polymer backbone, resulting in materials with enhanced thermal stability, mechanical properties, or chemical resistance.Overall, trimethyl(pent-1-yn-1-yl)silane plays a crucial role in the advancement of chemical synthesis by enabling the efficient construction of silicon-containing compounds and materials with diverse functionalities and applications.