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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, (4-chlorophenyl)trimethyl-

Clc1ccc(cc1)[Si](C)(C)C Request for Quotation
Chemical Name: Silane, (4-chlorophenyl)trimethyl-
CAS Number: 10557-71-8
Product Number: AG003E84(AGN-PC-0JL74W)
Synonyms:
MDL No:
Molecular Formula: C9H13ClSi
Molecular Weight: 184.73802

Identification/Properties

Properties
Form:
Liquid
Computed Properties
Molecular Weight:
184.738g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
184.048g/mol
Monoisotopic Mass:
184.048g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
120
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


P-chlorophenyltrimethylsilane is a versatile organosilicon compound commonly used in chemical synthesis as a chlorinating agent. It plays a crucial role in reactions where selective introduction of a chloro group is required. This reagent is particularly effective in converting hydroxyl groups to chlorides, making it an essential tool in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and materials science. Its high reactivity and compatibility with a wide range of functional groups make it a valuable asset in the arsenal of synthetic chemists.