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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, 4-(4-iodophenyl)-

Ic1ccc(cc1)c1ccncc1 Request for Quotation
Chemical Name: Pyridine, 4-(4-iodophenyl)-
CAS Number: 83420-59-1
Product Number: AG0054GH(AGN-PC-09T1O5)
Synonyms:
MDL No:
Molecular Formula: C11H8IN
Molecular Weight: 281.0924

Identification/Properties

Properties
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Pyridine, 4-(4-iodophenyl)- is a valuable chemical reagent commonly utilized in organic synthesis processes. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and functional materials. Its unique chemical structure and reactivity make it particularly useful in the formation of complex molecular structures. By participating in a range of chemical reactions, Pyridine, 4-(4-iodophenyl)- enables the synthesis of diverse compounds with specific properties and functions, contributing significantly to the advancement of chemical research and development.