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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-iodo-1H-quinazoline-2,4-dione

O=c1[nH]c2c(I)cccc2c(=O)[nH]1 Request for Quotation
Chemical Name: 8-iodo-1H-quinazoline-2,4-dione
CAS Number: 959236-79-4
Product Number: AG006A8F(AGN-PC-0NP8KY)
Synonyms:
MDL No:
Molecular Formula: C8H5IN2O2
Molecular Weight: 288.0420

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
288.044g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
287.94g/mol
Monoisotopic Mass:
287.94g/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-Iodoquinazoline-2,4(1H,3H)-dione is a versatile compound widely utilized in chemical synthesis. It serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties. This compound is particularly valuable in organic synthesis as it can undergo various transformations, such as substitution reactions and cyclization processes, to yield complex molecular structures efficiently. Its ability to introduce the iodo group into organic molecules makes it a key intermediate in the preparation of bioactive compounds and functional materials. Additionally, its presence in a molecule can enhance the biological activity or alter the physicochemical properties, making it a crucial component in the development of new chemical entities.