Other grades of this product :
| 4-CHLORO-2-PHENYLQUINAZOLINE Basic information |
| 4-CHLORO-2-PHENYLQUINAZOLINE Chemical Properties |
| Melting point | 124-126 °C(lit.) | | Boiling point | 383.11°C (rough estimate) | | density | 1.285 | | refractive index | 1.5749 (estimate) | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | form | Crystalline Powder | | pka | 0.67±0.30(Predicted) | | color | Slightly yellow to yellow | | InChIKey | OBHKONRNYCDRKM-UHFFFAOYSA-N | | CAS DataBase Reference | 6484-25-9(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 37/39-26 | | WGK Germany | 3 | | HS Code | 29339980 |
| 4-CHLORO-2-PHENYLQUINAZOLINE Usage And Synthesis |
| Chemical Properties | slightly yellow to yellow crystalline powder | | Uses | 4-Chloro-2-phenylquinazoline can be involved in the synthesis of biologically active molecules including: Nitrotriazole amines or nitroimidazole amines for use as antitrypanosomal activity and mammalian cytotoxicity.
| | Uses | Reactant involved in the synthesis of biologically active molecules including:- Nitrotriazole amines or nitroimidazole amines for use as antitrypanosomal activity and mammalian cytotoxicity
- Quinazoline-containing piperazinylpyrimidine derivatives with antitumor activity
- Quinazoline substituted cyclopentane as HCV NS3/4A protease inhibitors
- Quinazolines with antibacterial and antitumor activity
- Aurora inhibitor MK-0457
Reactant involved in Suzuki-Miyaura cross-coupling and catalyst-free / base-free water promoted nucleophilic aromatic substitution | | Synthesis Reference(s) | Journal of the American Chemical Society, 68, p. 1299, 1946 DOI: 10.1021/ja01211a055 |
| 4-CHLORO-2-PHENYLQUINAZOLINE Preparation Products And Raw materials |
|
日本语
한국어
Français
Deutsch
España
Türkiye