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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-Pyridinecarbonyl chloride, 2,6-dichloro-5-fluoro-

ClC(=O)c1cc(F)c(nc1Cl)Cl Request for Quotation
Chemical Name: 3-Pyridinecarbonyl chloride, 2,6-dichloro-5-fluoro-
CAS Number: 96568-02-4
Product Number: AG006712(AGN-PC-0KK65Z)
Synonyms:
MDL No:
Molecular Formula: C6HCl3FNO
Molecular Weight: 228.4356

Identification/Properties

Computed Properties
Molecular Weight:
228.428g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
226.911g/mol
Monoisotopic Mass:
226.911g/mol
Topological Polar Surface Area:
30A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
192
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


3-Pyridinecarbonylchloride, 2,6-dichloro-5-fluoro- is a versatile chemical compound widely used in organic synthesis processes. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique chemical structure allows it to participate in a variety of reactions, making it a valuable tool for chemists and researchers.In chemical synthesis, 3-Pyridinecarbonylchloride, 2,6-dichloro-5-fluoro- can be utilized as an acyl chloride reagent, facilitating the introduction of the pyridine ring and halogen substituents into target molecules. This compound is particularly valuable in the synthesis of heterocyclic compounds, where its reactivity and selectivity play a crucial role in controlling the regioselectivity and stereochemistry of the final products.Furthermore, 3-Pyridinecarbonylchloride, 2,6-dichloro-5-fluoro- can also be employed as a precursor for the preparation of various functionalized pyridine derivatives. By judiciously choosing reaction conditions and suitable reagents, chemists can leverage the versatility of this compound to access a wide range of complex molecules with diverse biological activities and industrial applications.