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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, tributyl-

CCCC[SiH](CCCC)CCCC Request for Quotation
Chemical Name: Silane, tributyl-
CAS Number: 998-41-4
Product Number: AG003V07(AGN-PC-0JO23C)
Synonyms:
MDL No:
Molecular Formula: C12H28Si
Molecular Weight: 200.43622

Identification/Properties

Properties
BP:
225-226°C at 755 mmHg
Storage:
2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
199.433g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
9
Exact Mass:
199.188g/mol
Monoisotopic Mass:
199.188g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
72.1
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-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P370+P378-P403+P235-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tributylsilane is a versatile compound commonly utilized in chemical synthesis as a reducing agent and a source of silicon in various reactions. Its ability to donate hydride ions makes it particularly valuable in organic transformations, where it is often employed to reduce functional groups such as ketones, aldehydes, and alkenes. This reagent is known for its high selectivity and mild reaction conditions, making it a preferred choice in complex synthesis routes. Furthermore, tributylsilane can also serve as a protecting group for alcohols and amines, enabling chemists to selectively modify specific functional groups within a molecule. Its compatibility with a wide range of solvents and other reagents further enhances its utility in organic synthesis, making it an indispensable tool for chemists working in various research and industrial settings.