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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, bromotriethyl-

CC[Si](CC)(CC)Br Request for Quotation
Chemical Name: Silane, bromotriethyl-
CAS Number: 1112-48-7
Product Number: AG003OKT(AGN-PC-0JL9UY)
Synonyms:
MDL No:
Molecular Formula: C6H15BrSi
Molecular Weight: 195.1728

Identification/Properties

Properties
MP:
-50℃
Storage:
Room Temperature;Inert atmosphere;
Form:
Liquid
Computed Properties
Molecular Weight:
195.175g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
3
Exact Mass:
194.013g/mol
Monoisotopic Mass:
194.013g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
51.3
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


Triethylbromosilane is a versatile chemical reagent commonly used in organic synthesis. As a bromosilane compound, it plays a crucial role in various chemical reactions due to its unique properties. In the field of chemical synthesis, Triethylbromosilane is primarily employed as a key intermediate in the preparation of organosilicon compounds. By acting as a source of both silicon and bromine atoms, it facilitates the introduction of silicon-containing functional groups into a wide range of organic molecules. This reagent is particularly valuable in the formation of silicon-carbon bonds, a fundamental step in the synthesis of organosilicon compounds with diverse applications in materials science, pharmaceuticals, and agrochemicals. Additionally, Triethylbromosilane can serve as a protecting group for alcohols and amines, enabling selective transformations in complex molecules. Its versatility and reactivity make Triethylbromosilane an indispensable tool for chemists seeking to access novel silicon-containing compounds with tailored properties.