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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, tripropyl-

CCC[SiH](CCC)CCC Request for Quotation
Chemical Name: Silane, tripropyl-
CAS Number: 998-29-8
Product Number: AG003W7I(AGN-PC-0JL9PM)
Synonyms:
MDL No:
Molecular Formula: C9H22Si
Molecular Weight: 158.3565

Identification/Properties

Properties
BP:
171 °C(lit.)
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
157.352g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
6
Exact Mass:
157.141g/mol
Monoisotopic Mass:
157.141g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
47.5
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


Tripropylsilane, a versatile organosilicon compound, finds extensive applications in chemical synthesis as a valuable reducing agent and a silylating agent. Its primary role lies in its ability to transfer hydrosilane groups to a wide variety of organic substrates. This enables the reduction of various functional groups such as ketones, aldehydes, and olefins, making it an essential tool in organic chemistry. Additionally, Tripropylsilane is commonly used in the silylation of alcohols, amines, and carboxylic acids, facilitating further chemical transformations. Its high reactivity and selectivity make it a go-to reagent for synthetic chemists looking to efficiently introduce silicon functionalities into complex molecular structures.