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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, 3-iodo-2-(trifluoromethyl)-

Ic1cccnc1C(F)(F)F Request for Quotation
Chemical Name: Pyridine, 3-iodo-2-(trifluoromethyl)-
CAS Number: 590371-71-4
Product Number: AG00EAGA(AGN-PC-050B64)
Synonyms:
MDL No:
Molecular Formula: C6H3F3IN
Molecular Weight: 272.9944

Identification/Properties

Computed Properties
Molecular Weight:
272.997g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
272.926g/mol
Monoisotopic Mass:
272.926g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
136
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H320-H335
Precautionary Statements:
P264-P270-P301+P312-P330
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Iodo-2-(trifluoromethyl)pyridine is a versatile compound widely used in chemical synthesis. One of its key applications is as a reagent in the functionalization of aromatic compounds. Due to the presence of both an iodo group and a trifluoromethyl group, this compound serves as a powerful building block for creating new molecules with unique properties.In organic synthesis, 3-Iodo-2-(trifluoromethyl)pyridine can act as a nucleophilic source of iodine, allowing for the introduction of an iodo group onto various organic substrates. The trifluoromethyl group enhances the reactivity and stability of the compound, making it an efficient tool for forming carbon-carbon and carbon-heteroatom bonds.Furthermore, 3-Iodo-2-(trifluoromethyl)pyridine can participate in cross-coupling reactions to access biologically active compounds, pharmaceutical intermediates, and agrochemicals. Its unique structure imparts desirable properties to the products, such as improved lipophilicity, metabolic stability, and bioavailability.Overall, the strategic placement of iodine and trifluoromethyl groups in 3-Iodo-2-(trifluoromethyl)pyridine makes it a valuable reagent in modern synthetic chemistry, enabling the efficient construction of complex molecules with diverse applications in drug discovery, material science, and crop protection.