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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, 5-bromo-3-chloro-

Clc1cc(Br)c[nH]c1=O Request for Quotation
Chemical Name: 2(1H)-Pyridinone, 5-bromo-3-chloro-
CAS Number: 58236-70-7
Product Number: AG00IAD6(AGN-PC-025WJ6)
Synonyms:
MDL No:
Molecular Formula: C5H3BrClNO
Molecular Weight: 208.4404

Identification/Properties

Properties
MP:
199-202℃
BP:
303.8°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
208.439g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
206.909g/mol
Monoisotopic Mass:
206.909g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
209
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-3-chloropyridin-2(1H)-one is a powerful building block in chemical synthesis that finds wide applications in organic chemistry. This compound is commonly used as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other important organic compounds.In organic synthesis, 5-Bromo-3-chloropyridin-2(1H)-one serves as a versatile starting material for the introduction of various functional groups through substitution or addition reactions. Its unique combination of bromine and chlorine substituents on a pyridine ring provides control over regioselectivity and reactivity, making it a valuable tool for creating structurally diverse molecules.One important application of 5-Bromo-3-chloropyridin-2(1H)-one is in the synthesis of heterocyclic compounds, where it can be used as a precursor for the construction of complex ring systems. By functionalizing the pyridine ring, chemists can tailor the properties of the resulting molecules for specific purposes, such as in drug discovery or materials science.Overall, the versatility and reactivity of 5-Bromo-3-chloropyridin-2(1H)-one make it an indispensable building block in modern chemical synthesis, enabling the efficient and strategic construction of a wide range of organic molecules with diverse applications.