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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, (3-bromophenyl)trimethyl-

Brc1cccc(c1)[Si](C)(C)C Request for Quotation
Chemical Name: Silane, (3-bromophenyl)trimethyl-
CAS Number: 17878-47-6
Product Number: AG0026B1(AGN-PC-0L6IF7)
Synonyms:
MDL No:
Molecular Formula: C9H13BrSi
Molecular Weight: 229.1890

Identification/Properties

Properties
BP:
50°C/0.5mmHg(lit.)
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Refractive Index:
n20/D1.532
Computed Properties
Molecular Weight:
229.192g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
227.997g/mol
Monoisotopic Mass:
227.997g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
11
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H413
Precautionary Statements:
P273
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(3-Bromophenyl)trimethylsilane, commonly used in chemical synthesis, serves as a versatile reagent due to its unique properties. This compound is frequently employed as a key building block in the synthesis of various organic compounds, such as pharmaceuticals, agrochemicals, and advanced materials. Its ability to easily undergo substitution reactions, particularly with nucleophiles, makes it a valuable tool for introducing the (3-bromophenyl) group into target molecules. Additionally, the trimethylsilyl functional group enhances the reactivity and stability of the compound in a wide range of synthetic transformations. This compound has found particular utility in the preparation of biologically active compounds and functional materials, making it an essential component in the toolbox of synthetic chemists.