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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)-

Stannane, tributyl-3-thienyl-

CCCC[Sn](c1cscc1)(CCCC)CCCC Request for Quotation
Chemical Name: Stannane, tributyl-3-thienyl-
CAS Number: 119405-65-1
Product Number: AG000IQA(AGN-PC-0NDISA)
Synonyms:
MDL No:
Molecular Formula: C16H30SSn
Molecular Weight: 373.1754

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Chemical Structure


Tributyl(thiophen-3-yl)stannane is a versatile organotin compound widely used in chemical synthesis for various applications. In organic chemistry, it serves as a valuable reagent for the introduction of thiophene-3-yl groups into organic molecules. This compound is commonly employed in Stille coupling reactions, where it participates in forming carbon-carbon bonds through cross-coupling reactions with various electrophiles such as aryl halides or pseudohalides. The incorporation of the thiophen-3-yl moiety into organic frameworks can impart unique electronic and structural properties, making Tributyl(thiophen-3-yl)stannane a valuable tool for the synthesis of functionalized organic compounds with diverse applications in materials science, pharmaceuticals, and agrochemicals. Moreover, its compatibility with a wide range of functional groups and mild reaction conditions make it a preferred reagent for organic chemists seeking to streamline synthetic pathways and access complex molecular architectures efficiently.