- Quinazoline derivatives as antitumor agents and their preparation, World Intellectual Property Organization, , ,
Cas no 944742-29-4 (5-Fluoro-7-methoxyquinazolin-4(3H)-one)
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
- Signal Word:Warning
- Hazard Statement: H302-H315-H319-H335
- Warning Statement: P261-P305+P351+P338
- Storage Condition:Sealed in dry,Room Temperature
5-Fluoro-7-methoxyquinazolin-4(3H)-one Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | F893308-1g |
5-Fluoro-7-methoxyquinazolin-4(3H)-one |
944742-29-4 | 97% | 1g |
660.60 | 2021-05-17 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-ES813-250mg |
5-Fluoro-7-methoxyquinazolin-4(3H)-one |
944742-29-4 | 97% | 250mg |
436CNY | 2021-05-08 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-ES813-100mg |
5-Fluoro-7-methoxyquinazolin-4(3H)-one |
944742-29-4 | 97% | 100mg |
157CNY | 2021-05-08 | |
| Chemenu | CM219299-1g |
5-Fluoro-7-methoxyquinazolin-4(3H)-one |
944742-29-4 | 97% | 1g |
$327 | 2021-08-04 | |
| ChemScence | CS-0038611-1g |
5-Fluoro-7-methoxyquinazolin-4(3H)-one |
944742-29-4 | ≥97.0% | 1g |
$101.0 | 2022-04-26 | |
| Alichem | A189011920-1g |
5-Fluoro-7-methoxyquinazolin-4(3H)-one |
944742-29-4 | 97% | 1g |
$385.00 | 2023-08-31 | |
| Alichem | A189011920-5g |
5-Fluoro-7-methoxyquinazolin-4(3H)-one |
944742-29-4 | 97% | 5g |
$1274.00 | 2023-08-31 | |
| Apollo Scientific | PC32957-100mg |
5-Fluoro-7-methoxy-4(3H)-quinazolinone |
944742-29-4 | 100mg |
£60.00 | 2025-02-21 | ||
| Apollo Scientific | PC32957-250mg |
5-Fluoro-7-methoxy-4(3H)-quinazolinone |
944742-29-4 | 250mg |
£95.00 | 2025-02-21 | ||
| Apollo Scientific | PC32957-1g |
5-Fluoro-7-methoxy-4(3H)-quinazolinone |
944742-29-4 | 1g |
£240.00 | 2025-02-21 |
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
1.2 Solvents: Water ; pH 5 - 6, 0 °C
Reference
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
1.2 Reagents: Water ; cooled
Reference
- Preparation of piperidinylmethoxyquinazolinylaminopyrazolylacetamides as aurora kinase inhibitors., World Intellectual Property Organization, , ,
Production Method 3
Reaction Conditions
1.1 Reagents: Sulfuric acid ; rt; 1 h, 100 °C
Reference
- Preparation of cyclopropyl fused 1,3-oxazin-2-amine compounds as beta-secretase inhibitors and methods of use, World Intellectual Property Organization, , ,
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, World Intellectual Property Organization, , ,
Production Method 7
Reaction Conditions
1.1 Reagents: Sulfuric acid Solvents: Water ; rt; 1 h, 100 °C
Reference
- Preparation of perfluorinated 5,6-dihydro-4H-1,3-oxazin-2-amine compounds as β-secretase inhibitors and methods of use, World Intellectual Property Organization, , ,
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
1.2 Reagents: Water ; cooled
Reference
- Fused multi-cyclic sulfone compounds as inhibitors of beta-secretase and methods of use and preparation thereof, United States, , ,
5-Fluoro-7-methoxyquinazolin-4(3H)-one Raw materials
5-Fluoro-7-methoxyquinazolin-4(3H)-one Preparation Products
5-Fluoro-7-methoxyquinazolin-4(3H)-one Related Literature
-
Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
-
Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622
-
Erika A. Cobar,Paul R. Horn,Robert G. Bergman,Martin Head-Gordon Phys. Chem. Chem. Phys., 2012,14, 15328-15339
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