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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)-Quinolinone, 6-iodo-

Ic1ccc2c(c1)ccc(=O)[nH]2 Request for Quotation
Chemical Name: 2(1H)-Quinolinone, 6-iodo-
CAS Number: 99455-01-3
Product Number: AG0036NE(AGN-PC-00O69C)
Synonyms:
MDL No:
Molecular Formula: C9H6INO
Molecular Weight: 271.0545

Identification/Properties

Properties
BP:
430.3°C at 760 mmHg
Storage:
2-8℃;Light sensitive;
Form:
Solid
Computed Properties
Molecular Weight:
271.057g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
270.949g/mol
Monoisotopic Mass:
270.949g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
227
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


6-Iodo-1H-Quinolin-2-One, also known as $name$, is a versatile compound widely used in chemical synthesis processes. With its unique structure and reactivity, $name$ serves as a valuable building block for the creation of various pharmaceuticals, agrochemicals, and materials.One key application of $name$ in chemical synthesis is as a precursor for the synthesis of complex heterocyclic compounds. By utilizing the iodo group as a reactive site, chemists can selectively modify the quinoline ring to introduce new functional groups or stereochemical elements. This versatility allows for the efficient construction of diverse molecular structures with specific properties and biological activities.Additionally, 6-Iodo-1H-Quinolin-2-One can act as a valuable starting material for the preparation of drug candidates and lead compounds in medicinal chemistry research. Through strategic derivatization and transformation reactions, researchers can explore the structure-activity relationships of novel molecules and optimize their biological profiles for potential therapeutic applications.Furthermore, the incorporation of $name$ into synthetic routes enables the streamlined and efficient synthesis of target molecules with higher yields and selectivity. Its reactivity and compatibility with various reaction conditions make it a useful tool for organic chemists seeking to access complex chemical architectures in a controlled manner.Overall, the application of 6-Iodo-1H-Quinolin-2-One in chemical synthesis offers a wide range of possibilities for designing and synthesizing novel compounds with tailored properties and functions, making it a valuable resource for advancing research and development in the fields of drug discovery, materials science, and beyond.