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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)-

Butanenitrile, 4-(trichlorosilyl)-

N#CCCC[Si](Cl)(Cl)Cl Request for Quotation
Chemical Name: Butanenitrile, 4-(trichlorosilyl)-
CAS Number: 1071-27-8
Product Number: AG003JCH(AGN-PC-0JKBJ6)
Synonyms:
MDL No:
Molecular Formula: C4H6Cl3NSi
Molecular Weight: 202.54164

Identification/Properties

Properties
BP:
237.5°C
Form:
Liquid
Computed Properties
Molecular Weight:
202.534g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
200.934g/mol
Monoisotopic Mass:
200.934g/mol
Topological Polar Surface Area:
23.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
122
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


3-Cyanopropyltrichlorosilane is a versatile intermediate used in chemical synthesis for a variety of applications. This compound is commonly employed as a crucial building block in the synthesis of silane-based coupling agents, which are essential in the modification of surfaces to enhance adhesion and compatibility in various industrial processes. Additionally, 3-Cyanopropyltrichlorosilane plays a key role in the development of functionalized silicon polymers, which find extensive use in coatings, adhesives, and specialty materials. Its ability to react with a range of nucleophiles further expands its utility in creating tailored molecules with specific functionalities for diverse applications in organic synthesis.