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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)-

9(10H)-Acridinone, 2-chloro-

Clc1ccc2c(c1)c(=O)c1c([nH]2)cccc1 Request for Quotation
Chemical Name: 9(10H)-Acridinone, 2-chloro-
CAS Number: 7497-52-1
Product Number: AG003H1C(AGN-PC-0JR97N)
Synonyms:
MDL No:
Molecular Formula: C13H8ClNO
Molecular Weight: 229.6617

Identification/Properties

Properties
BP:
394.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
229.663g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
229.029g/mol
Monoisotopic Mass:
229.029g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
294
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


2-Chloroacridin-9(10H)-one is a versatile compound widely utilized in chemical synthesis. Its unique structure and reactivity make it a valuable building block for the creation of various organic compounds. In the field of medicinal chemistry, 2-Chloroacridin-9(10H)-one is commonly employed in the synthesis of pharmaceutical agents and bioactive molecules. It serves as a key intermediate in the development of potential drug candidates due to its ability to undergo diverse chemical transformations, allowing for the introduction of functional groups and structural modifications essential for enhancing biological activity. Additionally, 2-Chloroacridin-9(10H)-one can be used in the preparation of fluorescent dyes, agrochemicals, and materials with specific properties. Its compatibility with a range of synthetic methodologies and its efficacy in generating complex molecular architectures highlight its significance in advancing chemical research and applications.