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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)-

2-(4-bicyclo[2.2.1]hept-2-enyl)ethyl-trichlorosilane

Cl[Si](CCC12CCC(C2)C=C1)(Cl)Cl Request for Quotation
Chemical Name: 2-(4-bicyclo[2.2.1]hept-2-enyl)ethyl-trichlorosilane
CAS Number: 54076-73-2
Product Number: AG00DC9G(AGN-PC-03O1CB)
Synonyms:
MDL No: MFCD08276258
Molecular Formula: C9H13Cl3Si
Molecular Weight: 255.64402

Identification/Properties

Computed Properties
Molecular Weight:
255.638g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
253.985g/mol
Monoisotopic Mass:
253.985g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
221
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
3
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 (2-(Bicyclo[2.2.1]hept-5-en-2-yl)ethyl)trichlorosilane is a versatile chemical reagent commonly utilized in organic synthesis for its unique properties. This compound functions as a valuable intermediate in the preparation of various functionalized organosilanes and silicon-based compounds. In chemical synthesis, it serves as a crucial building block in the creation of complex organic molecules with specific structural characteristics. Its reactivity towards nucleophiles and electrophiles allows for the selective modification of organic molecules, enabling the creation of new compounds with tailored properties. Additionally, the presence of trichlorosilane groups in the molecule facilitates its use as a coupling agent in the formation of C-Si bonds, offering a pathway for diversifying chemical structures. Furthermore, the bicyclic nature of the compound confers steric and electronic influences that can impact the reactivity and selectivity of the reactions it participates in, making it a valuable tool for synthetic chemists seeking to access novel compounds with intricate structures.