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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)-

5-iodo-4-methyl-2-(trifluoromethyl)pyridine

Ic1cnc(cc1C)C(F)(F)F Request for Quotation
Chemical Name: 5-iodo-4-methyl-2-(trifluoromethyl)pyridine
CAS Number: 944317-55-9
Product Number: AG00II5O(AGN-PC-0H8IRC)
Synonyms:
MDL No:
Molecular Formula: C7H5F3IN
Molecular Weight: 287.0209796

Identification/Properties

Computed Properties
Molecular Weight:
287.024g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
286.942g/mol
Monoisotopic Mass:
286.942g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
159
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


5-Iodo-4-methyl-2-(trifluoromethyl)pyridine is a versatile chemical compound widely utilized in chemical synthesis reactions. This specific compound plays a crucial role in organic chemistry as a valuable building block for the creation of complex molecules with unique properties. Its incorporation into various synthetic pathways enables the introduction of specific functionalities that are essential for the development of novel materials, pharmaceuticals, and agrochemicals. In particular, the trifluoromethyl and iodo substituents present in 5-Iodo-4-methyl-2-(trifluoromethyl)pyridine offer distinct reactivity profiles that can be leveraged to introduce fluorinated motifs and functional groups into target molecules. This compound's strategic placement within a synthetic route can facilitate the optimization of desired molecular structures and properties, making it a valuable tool for chemists in the pursuit of innovative chemical solutions.