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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)-Quinazolinone, 4-phenyl-

O=c1[nH]c2ccccc2c(n1)c1ccccc1 Request for Quotation
Chemical Name: 2(1H)-Quinazolinone, 4-phenyl-
CAS Number: 23441-75-0
Product Number: AG002N8A(AGN-PC-0JL5JF)
Synonyms:
MDL No:
Molecular Formula: C14H10N2O
Molecular Weight: 222.2420

Identification/Properties

Properties
MP:
254 - 257°C
Storage:
-10 ℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
222.247g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
222.079g/mol
Monoisotopic Mass:
222.079g/mol
Topological Polar Surface Area:
41.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
331
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Phenylquinazolin-2(1H)-one, a versatile heterocyclic compound, finds significant application in chemical synthesis as a key intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structural properties make it an invaluable building block for organic chemists seeking to design and develop novel molecules with diverse biological activities.In chemical synthesis, 4-Phenylquinazolin-2(1H)-one serves as a crucial precursor for the preparation of biologically active compounds such as anticancer agents, antimicrobial agents, and anti-inflammatory drugs. Its adaptable nature allows for functionalization at multiple sites, enabling the modification of its pharmacological properties to tailor specific applications.Furthermore, the synthetic versatility of 4-Phenylquinazolin-2(1H)-one facilitates the construction of complex molecular frameworks through various reactions such as condensation, substitution, and cyclization processes. This compound's role as a strategic intermediate underscores its importance in the development of potential drug candidates and innovative chemical entities with therapeutic potential.Overall, the use of 4-Phenylquinazolin-2(1H)-one in chemical synthesis highlights its significance as a foundational scaffold for the creation of diverse bioactive molecules, showcasing its utility and importance in modern organic chemistry research and pharmaceutical development.