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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)-

3,5-dichloro-4-fluoropyridine

Clc1cncc(c1F)Cl Request for Quotation
Chemical Name: 3,5-dichloro-4-fluoropyridine
CAS Number: 916791-62-3
Product Number: AG006R9P(AGN-PC-0NP8F2)
Synonyms:
MDL No:
Molecular Formula: C5H2Cl2FN
Molecular Weight: 165.9805

Identification/Properties

Properties
BP:
183.8 °C at 760 mmHg
Storage:
-10 ℃;
Computed Properties
Molecular Weight:
165.976g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
164.955g/mol
Monoisotopic Mass:
164.955g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
91
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


The 3,5-Dichloro-4-fluoropyridine is a versatile compound commonly used in chemical synthesis as a building block for various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique molecular structure and reactivity make it a valuable intermediate in the production of a wide range of complex organic molecules.One of the key applications of 3,5-Dichloro-4-fluoropyridine is in the synthesis of pharmaceutical compounds, where it serves as a precursor for the introduction of fluorine and chlorine atoms into drug molecules. These halogen substituents can significantly impact the biological activity and pharmacokinetic properties of the final pharmaceutical products, making 3,5-Dichloro-4-fluoropyridine a crucial starting material for medicinal chemistry research.Additionally, this compound is utilized in the development of agrochemicals, where its fluorine and chlorine functionalities can enhance the pesticidal or herbicidal properties of the final products. By incorporating 3,5-Dichloro-4-fluoropyridine into the molecular structure of agrochemicals, researchers can fine-tune the bioactivity and environmental profile of these compounds, contributing to the advancement of sustainable agriculture practices.Moreover, 3,5-Dichloro-4-fluoropyridine finds applications in the synthesis of specialty chemicals and materials, where its halogenated pyridine framework imparts unique properties to the resulting products. Through controlled chemical transformations of 3,5-Dichloro-4-fluoropyridine, chemists can access a diverse array of functionalized compounds with tailored characteristics for various industrial applications, showcasing the versatility and utility of this key building block in chemical synthesis.