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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)-

4-(4-Ethynylphenyl)pyridine

C#Cc1ccc(cc1)c1ccncc1 Request for Quotation
Chemical Name: 4-(4-Ethynylphenyl)pyridine
CAS Number: 83420-57-9
Product Number: AG01WZC9()
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


4-(4-Ethynylphenyl)pyridine is a versatile compound commonly utilized in chemical synthesis due to its unique properties and reactivity. Its ethynyl group provides a valuable handle for further functionalization, making it a crucial building block in the creation of various organic molecules. This compound is particularly valued in the field of organic chemistry for its ability to participate in Sonogashira cross-coupling reactions, enabling the formation of complex structures through carbon-carbon bond formation. Additionally, 4-(4-Ethynylphenyl)pyridine can serve as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials with tailored properties. Its strategic placement of functional groups makes it a valuable tool for chemists seeking to design and construct intricate molecular architectures for a wide range of applications.