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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)-

Silanamine, 1-ethyl-N-(ethyldimethylsilyl)-1,1-dimethyl-

CC[Si](N[Si](CC)(C)C)(C)C Request for Quotation
Chemical Name: Silanamine, 1-ethyl-N-(ethyldimethylsilyl)-1,1-dimethyl-
CAS Number: 17882-94-9
Product Number: AG0026ET(AGN-PC-0JMR91)
Synonyms:
MDL No:
Molecular Formula: C8H23NSi2
Molecular Weight: 189.4459

Identification/Properties

Computed Properties
Molecular Weight:
189.449g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
4
Exact Mass:
189.137g/mol
Monoisotopic Mass:
189.137g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
107
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-Ethyl-N-(ethyldimethylsilyl)-1,1-dimethylsilanamine is a versatile compound frequently used in chemical synthesis applications. This compound plays a crucial role as a reagent in various organic reactions, especially in the formation of silicon-containing compounds. Its unique structure enables it to act as a source of both an amine and a silyl group, allowing for selective functionalization of organic molecules. In addition, 1-Ethyl-N-(ethyldimethylsilyl)-1,1-dimethylsilanamine is often employed in the synthesis of complex organic molecules and pharmaceutical intermediates due to its ability to introduce silicon atoms into the target molecules, imparting desirable properties and functionalities. Furthermore, this compound is known for its compatibility with a wide range of reaction conditions, making it a valuable tool for synthetic chemists seeking to create novel compounds with tailored properties.