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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)-

2(1H)-Pyridinone, 4-amino-3,5-dichloro-6-fluoro-

Fc1[nH]c(=O)c(c(c1Cl)N)Cl Request for Quotation
Chemical Name: 2(1H)-Pyridinone, 4-amino-3,5-dichloro-6-fluoro-
CAS Number: 94133-62-7
Product Number: AG006R6E(AGN-PC-0JNDKV)
Synonyms:
MDL No:
Molecular Formula: C5H3Cl2FN2O
Molecular Weight: 196.9945

Identification/Properties

Properties
BP:
134.7°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
196.99g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
195.961g/mol
Monoisotopic Mass:
195.961g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
284
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 4-Amino-3,5-dichloro-6-fluoropyridin-2(1H)-one compound is a versatile chemical intermediate commonly used in chemical synthesis processes. Its unique structure allows it to participate in a variety of reactions and transformations, making it a valuable building block for the creation of various organic compounds.In organic synthesis, 4-Amino-3,5-dichloro-6-fluoropyridin-2(1H)-one can be employed as a key component in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. It serves as a crucial starting material for the synthesis of heterocyclic compounds that exhibit diverse biological activities. Additionally, its fluorine and chlorine substituents provide strategic positions for further functionalization, enabling the introduction of additional chemical moieties to tailor the properties of the final product.By incorporating 4-Amino-3,5-dichloro-6-fluoropyridin-2(1H)-one into synthetic pathways, chemists can access a wide range of structurally complex molecules with desired properties. Its application extends across various industries, facilitating the development of novel compounds with potential therapeutic, agricultural, or industrial applications.