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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)-

2,4(1H,3H)-Quinazolinedione, 6-chloro-

Clc1ccc2c(c1)c(=O)[nH]c(=O)[nH]2 Request for Quotation
Chemical Name: 2,4(1H,3H)-Quinazolinedione, 6-chloro-
CAS Number: 1640-60-4
Product Number: AG001UL2(AGN-PC-0JOO6O)
Synonyms:
MDL No:
Molecular Formula: C8H5ClN2O2
Molecular Weight: 196.5905

Identification/Properties

Computed Properties
Molecular Weight:
196.59g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
196.004g/mol
Monoisotopic Mass:
196.004g/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


6-Chloroquinazoline-2,4(1H,3H)-dione, also known as $name$, is a versatile chemical compound widely used in chemical synthesis processes. This compound plays a crucial role in the pharmaceutical industry, where it is utilized as a key building block in the synthesis of various biologically active compounds and drug candidates. Due to its unique structure and reactivity, $name$ serves as a valuable precursor in the production of specialized organic molecules with potential therapeutic applications. In addition, it is employed in the development of novel materials and agrochemicals, demonstrating its significance across diverse fields of chemistry. With its distinct properties and synthetic capabilities, 6-Chloroquinazoline-2,4(1H,3H)-dione continues to be a fundamental component in the advancement of chemical synthesis methodologies and the creation of innovative compounds.