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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-(triethoxysilyl)-

CCO[Si](OCC)(OCC)CCCC#N Request for Quotation
Chemical Name: Butanenitrile, 4-(triethoxysilyl)-
CAS Number: 1067-47-6
Product Number: AG003JCI(AGN-PC-0JKBIC)
Synonyms:
MDL No:
Molecular Formula: C10H21NO3Si
Molecular Weight: 231.36414

Identification/Properties

Properties
BP:
239.3°C at 760 mmHg
Form:
Liquid
Stability:
Moisture Sensitive
Refractive Index:
n20/D 1.417(lit.)
Computed Properties
Molecular Weight:
231.367g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
9
Exact Mass:
231.129g/mol
Monoisotopic Mass:
231.129g/mol
Topological Polar Surface Area:
51.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
185
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:
H227-H315-H319
Precautionary Statements:
P210-P280-P305+P351+P338-P362-P403+P235-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (3-Cyanopropyl)triethoxysilane is a versatile compound widely used in chemical synthesis as a key intermediate in the production of various functional materials. As a silane coupling agent, it plays a crucial role in bonding organic material to inorganic surfaces. In the field of materials science, it is utilized in the modification of surfaces to enhance adhesion, improve surface properties, and provide compatibility between dissimilar materials. This compound is particularly valued for its ability to create strong bonds with both organic and inorganic substrates, making it an essential component in the manufacturing of adhesives, coatings, and composites. Its unique chemical structure enables precise control over surface interactions, leading to the development of advanced materials with tailored properties for a wide range of industrial applications. In organic synthesis, (3-Cyanopropyl)triethoxysilane serves as a valuable building block for the creation of complex molecules and polymers, enabling chemists to introduce functional groups and enhance the reactivity of organic compounds. Its compatibility with various reaction conditions and its ability to participate in a variety of chemical transformations make it a valuable tool for the synthesis of specialty chemicals, pharmaceuticals, and agrochemicals. Additionally, this compound is employed in the preparation of functionalized silica nanoparticles, which find applications in drug delivery systems, catalysis, and electronic devices. In summary, the (3-Cyanopropyl)triethoxysilane plays a pivotal role in chemical synthesis by enabling the modification of surfaces, the creation of new materials, and the synthesis of complex organic compounds, thereby contributing to advancements in diverse fields such as materials science, chemistry, and nanotechnology.