ChemicalBook > Product Catalog > Organic Chemistry > Heterocyclic Compounds > 4-CHLORO-2-PHENYLQUINAZOLINE
4-CHLORO-2-PHENYLQUINAZOLINE
4-CHLORO-2-PHENYLQUINAZOLINE Basic information
- Product Name:
- 4-CHLORO-2-PHENYLQUINAZOLINE
- Synonyms:
-
- AKOS 93518
- AM-EX-OL(R)
- 4-CHLORO-2-PHENYLQUINAZOLINE
- QUINAZOLINE, 4-CHLORO-2-PHENYL-
- 4-CHLORO-2-PHENYLQUINAZOLINE OR AM-ex-OL
- AM-EX-OL, 97% (4-CHLORO-2-PHENYL-QUINAZO LINE)
- am-ex-ol tm
- 4-CHLORO-2-PHENYLQUINAZOLINE 97%
- CAS:
- 6484-25-9
- MF:
- C14H9ClN2
- MW:
- 240.69
- EINECS:
- 229-346-2
- Product Categories:
-
- quinazoline
- Building Blocks
- Chemical Synthesis
- Halogenated Heterocycles
- Heterocyclic Building Blocks
- Quinazolines
- Mol File:
- 6484-25-9.mol
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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)
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MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
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4-CHLORO-2-PHENYLQUINAZOLINE Usage And Synthesis
Chemical Properties
slightly yellow to yellow crystalline powder
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
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.
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
Raw materials
4-CHLORO-2-PHENYLQUINAZOLINESupplier
J & K SCIENTIFIC LTD.
- Tel
- 010-82848833 400-666-7788
- jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
- Tel
- 021-61259108 18621169109
- market03@meryer.com
Energy Chemical
- Tel
- 021-021-58432009 400-005-6266
- sales8178@energy-chemical.com
Shanghai Yuanding Chem. Sci. & Tech. Co., Ltd.
- Tel
- 21-57721279
- sales@shydchem.com.cn
Pure Chemistry Scientific Inc.
- Tel
- 001-857-928-2050 or 1-888-588-9418
- sales@chemreagents.com
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4-CHLORO-2-PHENYLQUINAZOLINE(6484-25-9)Related Product Information
- 4-CHLORO-2-PHENYLQUINAZOLINE
- Oxazoline
- Quinazoline
- 4-CHLORO-2-(2-FLUORO-PHENYL)-QUINAZOLINE
- 2-(4-BROMO-PHENYL)-4-CHLORO-QUINAZOLINE
- QUINAZOLINE, 4-CHLORO-7-FLUORO-2-PHENYL-
- 4-CHLORO-2-(4-METHOXY-PHENYL)-QUINAZOLINE
- 4-CHLORO-2-(4-CHLORO-PHENYL)-QUINAZOLINE
- 4,6-DICHLORO-2-PHENYL-QUINAZOLINE
- 6-BROMO-4-CHLORO-2-PHENYL-QUINAZOLINE
- 4-chloro-2-(2-chlorophenyl)quinazoline
- QUINAZOLINE, 4-CHLORO-6-FLUORO-2-PHENYL-
- 4-CHLORO-2-(4-FLUORO-PHENYL)-QUINAZOLINE
- 4,7-DICHLORO-2-PHENYL-QUINAZOLINE
- 6-chloro-4-phenylquinazoline
- 6-BROMO-2-CHLORO-4-PHENYLQUINAZOLINE
- 4-CHLORO-2-(3-CHLORO-PHENYL)-QUINAZOLINE
- AURORA 19333