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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)-

Stannanamine, pentamethyl-

CN([Sn](C)(C)C)C Request for Quotation
Chemical Name: Stannanamine, pentamethyl-
CAS Number: 993-50-0
Product Number: AG003BZW(AGN-PC-0JLD0Q)
Synonyms:
MDL No:
Molecular Formula: C5H15NSn
Molecular Weight: 207.8803

Identification/Properties

Properties
MP:
1℃ [ALD94]
Form:
Liquid
Computed Properties
Molecular Weight:
207.892g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
209.023g/mol
Monoisotopic Mass:
209.023g/mol
Topological Polar Surface Area:
3.2A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
53.6
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


N,N,1,1,1-Pentamethylstannanamine is a versatile compound used in various chemical synthesis applications. This highly reactive organotin compound serves as a valuable reagent in organic chemistry, particularly in the synthesis of organotin and organosilicon compounds. Its unique structure, with pentamethyl substituents attached to the tin atom, imparts specific properties that make it useful in a range of chemical reactions.In chemical reactions, N,N,1,1,1-Pentamethylstannanamine can act as a nucleophile, attacking electrophilic centers to form new carbon-carbon or carbon-heteroatom bonds. Its reactivity and stability under certain conditions make it a preferred choice for introducing tin and methyl functionalities into organic molecules. Additionally, this compound can participate in complexation reactions, coordination chemistry, and catalytic processes, highlighting its significance in modern synthetic organic chemistry.Overall, N,N,1,1,1-Pentamethylstannanamine plays a crucial role as a building block in the development of new materials, pharmaceuticals, agrochemicals, and other fine chemicals. Its application in chemical synthesis extends to the production of specialty compounds with tailored properties, making it an essential tool for synthetic chemists seeking innovative pathways to novel molecules.