1. Home
  2. 3,5-Dibromo-2-fluoro-4-methylpyridine

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

3,5-Dibromo-2-fluoro-4-methylpyridine

Brc1cnc(c(c1C)Br)F Request for Quotation
Chemical Name: 3,5-Dibromo-2-fluoro-4-methylpyridine
CAS Number: 1000340-01-1
Product Number: AG0000DA(AGN-PC-058CRX)
Synonyms:
MDL No:
Molecular Formula: C6H4Br2FN
Molecular Weight: 268.9091

Identification/Properties

Computed Properties
Molecular Weight:
268.911g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
268.867g/mol
Monoisotopic Mass:
266.869g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
122
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

Request for Quotation

Customer Feedback

Chemical Structure


2-Fluoro-3,5-dibromo-4-methylpyridine is a versatile compound widely used in chemical synthesis due to its unique reactivity and structural properties. This compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. In particular, 2-Fluoro-3,5-dibromo-4-methylpyridine is utilized in the synthesis of complex organic molecules through diverse chemical reactions such as nucleophilic substitution, cross-coupling, and metal-catalyzed transformations. Its halogenated structure provides essential functionality for introducing specific groups or motifs into target compounds, allowing for precise diversification and modification. Furthermore, the presence of the fluorine atom imparts distinct physicochemical properties, influencing the compound's solubility, stability, and bioactivity. Overall, 2-Fluoro-3,5-dibromo-4-methylpyridine plays a crucial role in the advancement of modern synthetic chemistry by enabling the efficient construction of novel chemical entities with potential applications across various industries.