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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)-

Pyridine, 2-methyl-6-(tributylstannyl)-

CCCC[Sn](c1cccc(n1)C)(CCCC)CCCC Request for Quotation
Chemical Name: Pyridine, 2-methyl-6-(tributylstannyl)-
CAS Number: 259807-95-9
Product Number: AG002RAR(AGN-PC-009M1T)
Synonyms:
MDL No: MFCD07787401
Molecular Formula: C18H33NSn
Molecular Weight: 382.1623

Identification/Properties

Computed Properties
Molecular Weight:
382.179g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
10
Exact Mass:
383.164g/mol
Monoisotopic Mass:
383.164g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
220
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


2-Methyl-6-(tributylstannyl)pyridine is a versatile organotin compound widely used in chemical synthesis as a powerful reagent for the introduction of the tributylstannyl group onto various organic compounds. This functional group can serve as a key intermediate in divergent synthetic pathways, enabling the selective modification of complex molecules with high efficiency and precision. In the field of organic chemistry, 2-Methyl-6-(tributylstannyl)pyridine is particularly valued for its ability to facilitate cross-coupling reactions, such as palladium-catalyzed Stille coupling, enabling the construction of carbon-carbon and carbon-heteroatom bonds in a controlled manner. Additionally, this compound can act as a valuable building block in the synthesis of biologically active compounds, natural products, and advanced materials, making it an indispensable tool for synthetic chemists striving to achieve diverse molecular architectures with tailored properties.