推薦產品
化驗
97%
形狀
liquid
mp
124-126 °C (lit.)
SMILES 字串
Clc1nc(nc2ccccc12)-c3ccccc3
InChI
1S/C14H9ClN2/c15-13-11-8-4-5-9-12(11)16-14(17-13)10-6-2-1-3-7-10/h1-9H
InChI 密鑰
OBHKONRNYCDRKM-UHFFFAOYSA-N
應用
4-Chloro-2-phenylquinazoline was used in synthesis of axially chiral quinazoline-containing phosphinamine ligand, N,N,2-triphenylquinazolin-4-amine, sulfanyl and sulfinylbenzodiazines. It was used as reagent for the conversion of phenols to anilines.
Reactant involved in the synthesis of biologically active molecules including:
Reactant involved in Suzuki-Miyaura cross-coupling and catalyst-free / base-free water promoted nucleophilic aromatic substitution
- 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
法律資訊
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
The Journal of Organic Chemistry, 37, 1681-1681 (1972)
The Journal of Organic Chemistry, 29, 1893-1893 (1964)
The preparation and resolution of 2-phenyl-Quinazolinap, a new atropisomeric phosphinamine ligand for asymmetric catalysis.
McCarthy M, et al.
Tetrahedron Asymmetry, 10(14), 2797-2807 (1999)
A highly efficient red electrophosphorescent iridium (iii) complex containing phenyl quinazoline ligand in polymer light-emitting diodes.
Mei Q, et al.
Journal of Materials Chemistry, 22(14), 6878-6884 (2012)
Syntheses of sulfoxide derivatives in the benzodiazine series. Diazines. Part 37.
Le Fur N, et al.
Tetrahedron, 60(36), 7983-7994 (2004)
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