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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'-Biphenyl]-4-carbonitrile, 4'-hydroxy-3'-iodo-

N#Cc1ccc(cc1)c1ccc(c(c1)I)O Request for Quotation
Chemical Name: [1,1'-Biphenyl]-4-carbonitrile, 4'-hydroxy-3'-iodo-
CAS Number: 460746-47-8
Product Number: AG00D947(AGN-PC-0N355G)
Synonyms:
MDL No:
Molecular Formula: C13H8INO
Molecular Weight: 321.1132

Identification/Properties

Properties
MP:
166-167℃
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
321.117g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
320.965g/mol
Monoisotopic Mass:
320.965g/mol
Topological Polar Surface Area:
44A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
277
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


4'-Hydroxy-3'-iodo-[1,1'-biphenyl]-4-carbonitrile is a versatile compound commonly used in chemical synthesis as a key building block in the creation of various organic molecules. This compound plays a crucial role in the development of pharmaceuticals, agrochemicals, and materials science due to its unique structure and properties.In chemical synthesis, 4'-Hydroxy-3'-iodo-[1,1'-biphenyl]-4-carbonitrile serves as a valuable intermediate that can be further modified to introduce desired functional groups or structural motifs into the final product. The presence of the hydroxy group allows for facile derivatization, enabling the attachment of different chemical groups to tailor the compound's properties for specific applications.Additionally, the iodo group in 4'-Hydroxy-3'-iodo-[1,1'-biphenyl]-4-carbonitrile provides a convenient site for cross-coupling reactions, facilitating the synthesis of more complex molecules through bond formation with other organic substrates. This reactivity makes this compound an essential component in the construction of diverse chemical structures with varied functionalities.Overall, 4'-Hydroxy-3'-iodo-[1,1'-biphenyl]-4-carbonitrile is a valuable tool in the hands of synthetic chemists, offering versatility and control in the design and synthesis of novel compounds for pharmaceutical, agricultural, and materials applications.