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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)-

1,1':4',1''-Terphenyl, 2',5'-diiodo-

Ic1cc(c(cc1c1ccccc1)I)c1ccccc1 Request for Quotation
Chemical Name: 1,1':4',1''-Terphenyl, 2',5'-diiodo-
CAS Number: 96843-21-9
Product Number: AG006661(AGN-PC-00MFU1)
Synonyms:
MDL No:
Molecular Formula: C18H12I2
Molecular Weight: 482.0968

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
482.103g/mol
XLogP3:
6.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
481.903g/mol
Monoisotopic Mass:
481.903g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
262
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',5'-Diiodo-p-terphenyl is a versatile compound that finds its application in various chemical synthesis processes. Due to its unique structure and reactivity, this compound serves as a valuable building block for the creation of complex organic molecules. In organic synthesis, it is often used as a key reagent for the construction of biaryl compounds, which are essential components in pharmaceuticals, agrochemicals, and materials science.Furthermore, the presence of iodine atoms in 2',5'-Diiodo-p-terphenyl allows for facile derivatization reactions, enabling chemists to introduce additional functional groups or modify its structure to tailor its properties for specific applications. Its ability to undergo cross-coupling reactions, such as Suzuki-Miyaura coupling, Heck coupling, or Sonogashira coupling, makes it a valuable tool for the formation of carbon-carbon and carbon-heteroatom bonds.Overall, 2',5'-Diiodo-p-terphenyl plays a crucial role in modern organic synthesis by providing chemists with a powerful and versatile reagent for the construction of complex organic molecules with diverse applications.