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4-CHLORO-2-PHENYLQUINAZOLINE

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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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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26
WGK Germany 
3
HS Code 
29339980

MSDS

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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

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