Cas no 944742-29-4 (5-Fluoro-7-methoxyquinazolin-4(3H)-one)

5-Fluoro-7-methoxyquinazolin-4(3H)-one structure
944742-29-4 structure
Product Name:5-Fluoro-7-methoxyquinazolin-4(3H)-one
CAS No:944742-29-4
MF:C9H7FN2O2
MW:194.162485361099
MDL:MFCD13191851
CID:2600877
PubChem ID:135742289
Update Time:2024-10-25

5-Fluoro-7-methoxyquinazolin-4(3H)-one Chemical and Physical Properties

Names and Identifiers

    • 5-Fluoro-7-methoxyquinazolin-4(3H)-one
    • 5-fluoro-7-methoxy-4(3H)-Quinazolinone
    • NULL
    • 4(3H)-Quinazolinone, 5-fluoro-7-methoxy-
    • VWAQAXQCMOLAKY-UHFFFAOYSA-N
    • 5-fluoro-7-methoxyquinazolin-4-ol
    • BCP18476
    • AK341443
    • 5-fluoro-7-methoxy-1H-quinazolin-4-one
    • 5-Fluoro-7-methoxy-4(3H)-quinazolinone (ACI)
    • Cyclopropylmethanesulfonyl chloride
    • SCHEMBL2798284
    • DS-12275
    • MFCD13191851
    • SCHEMBL15900305
    • 5-fluoro-7-methoxy-3,4-dihydroquinazolin-4-one
    • CS-0038611
    • AKOS027338963
    • ZB1245
    • DB-107633
    • 5-fluoro-7-methoxy-3H-quinazolin-4-one
    • 944742-29-4
    • MDL: MFCD13191851
    • Inchi: 1S/C9H7FN2O2/c1-14-5-2-6(10)8-7(3-5)11-4-12-9(8)13/h2-4H,1H3,(H,11,12,13)
    • InChI Key: VWAQAXQCMOLAKY-UHFFFAOYSA-N
    • SMILES: O=C1C2C(=CC(=CC=2F)OC)NC=N1

Computed Properties

  • Exact Mass: 194.04915563g/mol
  • Monoisotopic Mass: 194.04915563g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 1
  • Complexity: 270
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 50.7
  • XLogP3: 0.8

Experimental Properties

  • Boiling Point: 333.7±52.0°C at 760 mmHg

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

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

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

Production Method 1

Reaction Conditions
1.1 Catalysts: Sulfuric acid Solvents: Water ;  3 h, 100 °C; 100 °C → rt
1.2 Solvents: Water ;  pH 5 - 6, 0 °C
Reference
Quinazoline derivatives as antitumor agents and their preparation
, World Intellectual Property Organization, , ,

Production Method 2

Reaction Conditions
1.1 Catalysts: Sulfuric acid Solvents: Water ;  20 min, rt; 5 h, 100 °C; 100 °C → rt
1.2 Reagents: Water ;  cooled
Reference
Preparation of piperidinylmethoxyquinazolinylaminopyrazolylacetamides as aurora kinase inhibitors.
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Production Method 3

Reaction Conditions
1.1 Reagents: Sulfuric acid ;  rt; 1 h, 100 °C
Reference
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Production Method 4

Reaction Conditions
1.1 Reagents: Sulfuric acid ;  1 h, 100 °C
Reference
Aminodihydrothiazine and aminodioxidodihydrothiazine compounds as beta-secretase antagonists and their preparation
, World Intellectual Property Organization, , ,

Production Method 5

Reaction Conditions
1.1 Reagents: Sulfuric acid ;  rt; 1 h, 100 °C
Reference
Cyclopropathiazin-2-amine compounds as beta-secretase inhibitors and their preparation
, World Intellectual Property Organization, , ,

Production Method 6

Reaction Conditions
1.1 Reagents: Sulfuric acid ;  rt; 1 h, 100 °C
Reference
Bridged bicyclic aminothiazine dioxide compounds as inhibitors of beta-secretase and their preparation
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Production Method 7

Reaction Conditions
1.1 Reagents: Sulfuric acid Solvents: Water ;  rt; 1 h, 100 °C
Reference
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Production Method 8

Reaction Conditions
1.1 Reagents: Sulfuric acid Solvents: Formic acid ;  1 h, 100 °C; 100 °C → rt
1.2 Reagents: Water ;  cooled
Reference
Fused multi-cyclic sulfone compounds as inhibitors of beta-secretase and methods of use and preparation thereof
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5-Fluoro-7-methoxyquinazolin-4(3H)-one Raw materials

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

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