1. Home
  2. 5-Fluoro-7-methoxyquinazolin-4(3H)-one

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

5-Fluoro-7-methoxyquinazolin-4(3H)-one

COc1cc2nc[nH]c(=O)c2c(c1)F Request for Quotation
Chemical Name: 5-Fluoro-7-methoxyquinazolin-4(3H)-one
CAS Number: 944742-29-4
Product Number: AG00II7A(AGN-PC-0WAMJF)
Synonyms:
MDL No: MFCD13191851
Molecular Formula: C9H7FN2O2
Molecular Weight: 194.1625

Identification/Properties

Computed Properties
Molecular Weight:
194.165g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
194.049g/mol
Monoisotopic Mass:
194.049g/mol
Topological Polar Surface Area:
50.7A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
270
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


5-Fluoro-7-methoxyquinazolin-4(3H)-one is a versatile building block in chemical synthesis, particularly in the pharmaceutical industry. Its unique molecular structure makes it a valuable intermediate for the synthesis of various biologically active compounds. One of the key applications of 5-Fluoro-7-methoxyquinazolin-4(3H)-one is in the development of novel pharmaceuticals. By utilizing this compound as a starting material, chemists can introduce specific functional groups and modify its structure to create new drug candidates with potential therapeutic effects. Its presence in the synthesis process can impart desired pharmacological properties to the final products, making it a crucial component in drug discovery research.Furthermore, 5-Fluoro-7-methoxyquinazolin-4(3H)-one serves as a key intermediate in the preparation of complex molecules with pharmacological relevance. Its strategic placement within the synthetic pathway allows for precise control over the chemical reactions and enables the formation of intricate molecular architectures. By incorporating this compound into the synthesis of target molecules, chemists can access diverse chemical space and explore novel structures with potential biological activities.Overall, the utilization of 5-Fluoro-7-methoxyquinazolin-4(3H)-one in chemical synthesis opens up a wide range of possibilities for creating new compounds with pharmaceutical applications. Its role as a versatile building block underscores its significance in organic chemistry and drug development, driving innovation in the field of medicinal chemistry.