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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-butyl-N,N,1,1-tetramethyl-

CCCC[Si](N(C)C)(C)C Request for Quotation
Chemical Name: Silanamine, 1-butyl-N,N,1,1-tetramethyl-
CAS Number: 181231-67-4
Product Number: AG0022QU(AGN-PC-0LAZ82)
Synonyms:
MDL No:
Molecular Formula: C8H21NSi
Molecular Weight: 159.3445

Identification/Properties

Computed Properties
Molecular Weight:
159.348g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
4
Exact Mass:
159.144g/mol
Monoisotopic Mass:
159.144g/mol
Topological Polar Surface Area:
3.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
89.3
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-Butyl-N,N,1,1-tetramethylsilanamine is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as an effective catalyst in various organic transformations, particularly in the functionalization of organic molecules containing reactive groups such as alcohols, amines, and acids. Its ability to promote selective reactions and facilitate the formation of complex molecular structures makes it an invaluable tool for chemists working in the field of synthesis. Furthermore, 1-Butyl-N,N,1,1-tetramethylsilanamine exhibits exceptional stability under a wide range of reaction conditions, allowing for efficient and reproducible transformations. Chemists rely on this compound to streamline their synthetic processes, enhance product yields, and access novel chemical entities with potential applications in pharmaceuticals, materials science, and other industries.