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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)-

8-fluoro-1H-quinazoline-2,4-dione

O=c1[nH]c2c(F)cccc2c(=O)[nH]1 Request for Quotation
Chemical Name: 8-fluoro-1H-quinazoline-2,4-dione
CAS Number: 959236-96-5
Product Number: AG00H6JM(AGN-PC-0MYFJP)
Synonyms:
MDL No: MFCD09954844
Molecular Formula: C8H5FN2O2
Molecular Weight: 180.1359

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Computed Properties
Molecular Weight:
180.138g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
180.034g/mol
Monoisotopic Mass:
180.034g/mol
Topological Polar Surface Area:
58.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
257
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


8-Fluoroquinazoline-2,4(1H,3H)-dione serves as a versatile building block in chemical synthesis, particularly in the pharmaceutical industry. This compound is commonly utilized for the development of novel drug candidates due to its unique structure and reactivity. In organic synthesis, 8-Fluoroquinazoline-2,4(1H,3H)-dione can undergo various transformations to introduce specific functional groups, enabling the creation of complex molecules with desired pharmacological properties. Its incorporation in medicinal chemistry projects allows for the exploration of diverse chemical space and the generation of potential candidates for therapeutic applications. By leveraging the synthetic versatility of 8-Fluoroquinazoline-2,4(1H,3H)-dione, researchers can efficiently access structurally diverse compounds for drug discovery efforts.