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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-methoxy-5-(tributylstannyl)-

CCCC[Sn](c1ccc(nc1)OC)(CCCC)CCCC Request for Quotation
Chemical Name: Pyridine, 2-methoxy-5-(tributylstannyl)-
CAS Number: 164014-93-1
Product Number: AG003N9J(AGN-PC-00EYR8)
Synonyms:
MDL No:
Molecular Formula: C18H33NOSn
Molecular Weight: 398.1617

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
398.178g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
11
Exact Mass:
399.158g/mol
Monoisotopic Mass:
399.158g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
238
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-Methoxy-5-(tributylstannyl)pyridine, often referred to as TBSP, is a versatile chemical compound widely utilized in organic synthesis procedures. This unique compound plays a crucial role in various chemical reactions due to its ability to act as a coupling agent. In chemical synthesis, TBSP is commonly employed as a key reagent in cross-coupling reactions to form carbon-carbon bonds between different organic molecules. This process is essential in the production of complex organic compounds, including pharmaceuticals, agrochemicals, and materials used in various industries. TBSP's high reactivity and selectivity make it an indispensable tool for chemists aiming to synthesize novel and structurally diverse compounds efficiently and effectively.