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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-Bromo-4-methyl-2-(trifluoromethyl)pyridine

Brc1cnc(cc1C)C(F)(F)F Request for Quotation
Chemical Name: 5-Bromo-4-methyl-2-(trifluoromethyl)pyridine
CAS Number: 1010422-51-1
Product Number: AG0003LT(AGN-PC-0HYI73)
Synonyms:
MDL No:
Molecular Formula: C7H5BrF3N
Molecular Weight: 240.0205

Identification/Properties

Computed Properties
Molecular Weight:
240.023g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
238.956g/mol
Monoisotopic Mass:
238.956g/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

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-4-methyl-2-(trifluoromethyl)pyridine is a versatile building block commonly used in chemical synthesis for the formation of complex organic compounds. This compound serves as a valuable tool in the construction of pharmaceuticals, agrochemicals, and materials due to its unique chemical properties and reactivity.In chemical synthesis, 5-Bromo-4-methyl-2-(trifluoromethyl)pyridine can act as a key intermediate in the preparation of various biologically active molecules. Its trifluoromethyl group enhances the compound's lipophilicity and electron-withdrawing ability, making it an important component in drug discovery and development. Additionally, the bromine atom provides a handle for further functionalization, allowing chemists to introduce specific structural modifications for target molecule optimization.Furthermore, the presence of the pyridine ring in 5-Bromo-4-methyl-2-(trifluoromethyl)pyridine imparts aromatic and basic properties, enabling it to participate in a wide range of organic reactions such as nucleophilic substitutions, cross-coupling reactions, and transition metal-catalyzed transformations. This molecule's diverse reactivity makes it a valuable building block for the synthesis of a variety of complex organic compounds with applications across different industries.Overall, the strategic incorporation of 5-Bromo-4-methyl-2-(trifluoromethyl)pyridine in chemical synthesis offers chemists a powerful tool for the efficient and controlled assembly of molecular frameworks with tailored properties and functionalities.