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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)-

(E)-3-trimethylsilylprop-2-en-1-amine

C=CCN[Si](C)(C)C Request for Quotation
Chemical Name: (E)-3-trimethylsilylprop-2-en-1-amine
CAS Number: 10519-97-8
Product Number: AG0085AT(AGN-PC-000YLR)
Synonyms:
MDL No:
Molecular Formula: C6H15NSi
Molecular Weight: 129.2755

Identification/Properties

Computed Properties
Molecular Weight:
129.278g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
129.097g/mol
Monoisotopic Mass:
129.097g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
73.1
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,1,1-Trimethyl-N-2-propen-1-ylsilanamine is a versatile compound that finds widespread application in chemical synthesis. This compound is commonly used as a reagent in organic chemistry reactions due to its unique chemical properties. Its ability to act as a nucleophile in reactions makes it valuable in the formation of various carbon-silicon bonds. Additionally, 1,1,1-Trimethyl-N-2-propen-1-ylsilanamine is often employed in the synthesis of organosilicon compounds, which have diverse applications in materials science and pharmaceutical chemistry. Its use as a building block in the preparation of functionalized silanes and silicon-containing polymers further highlights its significance in chemical synthesis.