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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)-

2-fluoro-3-iodo-6-(trifluoromethyl)pyridine

Ic1ccc(nc1F)C(F)(F)F Request for Quotation
Chemical Name: 2-fluoro-3-iodo-6-(trifluoromethyl)pyridine
CAS Number: 957345-34-5
Product Number: AG00H7PA(AGN-PC-0CPGBU)
Synonyms:
MDL No:
Molecular Formula: C6H2F4IN
Molecular Weight: 290.9849

Identification/Properties

Properties
BP:
208.562°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
290.987g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
0
Exact Mass:
290.917g/mol
Monoisotopic Mass:
290.917g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
160
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Fluoro-3-iodo-6-(trifluoromethyl)pyridine, a versatile building block in chemical synthesis, serves as a valuable intermediate in the creation of diverse compounds. With its unique fluorine and iodine substituents, this compound allows for the introduction of specific functional groups and modifications in target molecules. In organic synthesis, 2-Fluoro-3-iodo-6-(trifluoromethyl)pyridine can participate in various reactions such as cross-coupling reactions, nucleophilic substitution, and metal-catalyzed transformations. Its trifluoromethyl group enhances the compound's lipophilicity and metabolic stability, making it a desirable choice in medicinal chemistry for the development of potential drug candidates. Furthermore, the presence of fluorine and iodine atoms provides opportunities for radiolabeling and positron emission tomography (PET) imaging applications in chemical biology.