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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, (5-bromo-1-pentynyl)trimethyl-

BrCCCC#C[Si](C)(C)C Request for Quotation
Chemical Name: Silane, (5-bromo-1-pentynyl)trimethyl-
CAS Number: 66927-74-0
Product Number: AG006PSF(AGN-PC-0NG64R)
Synonyms:
MDL No:
Molecular Formula: C8H15BrSi
Molecular Weight: 219.1942

Identification/Properties

Computed Properties
Molecular Weight:
219.197g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
3
Exact Mass:
218.013g/mol
Monoisotopic Mass:
218.013g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
144
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


The (5-Bromopent-1-yn-1-yl)trimethylsilane compound serves as a valuable reagent in chemical synthesis processes, particularly in organic chemistry. Its unique structure containing both a bromine atom and a trimethylsilyl group allows for versatile applications in various reactions.One key use of (5-Bromopent-1-yn-1-yl)trimethylsilane is in Sonogashira coupling reactions, where it serves as an efficient alkynylation agent. This compound can effectively participate in cross-coupling reactions with various aryl or vinyl halides, providing a straightforward route to the synthesis of alkynes. By serving as a building block in such reactions, it enables the construction of complex molecular structures with precise control over the regioselectivity and stereochemistry of the resulting products.Furthermore, (5-Bromopent-1-yn-1-yl)trimethylsilane can also be utilized in the synthesis of heterocyclic compounds, such as pyrroles and pyridines, through multistep transformations. Its ability to undergo diverse chemical transformations makes it a valuable tool for the preparation of advanced organic molecules with potential applications in medicinal chemistry, materials science, and other research areas.