Basic information Uses Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Quinoline compounds >  2-CHLORO-4-PHENYLQUINAZOLINE

2-CHLORO-4-PHENYLQUINAZOLINE

Basic information Uses Safety Supplier Related

2-CHLORO-4-PHENYLQUINAZOLINE Basic information

Product Name:
2-CHLORO-4-PHENYLQUINAZOLINE
Synonyms:
  • 2-CHLORO-4-PHENYLQUIZOLINE
  • Quinazoline,2-chloro-4-phenyl-
  • 2-CHLORO-4-PHENYLQUINAZOLIN
  • oro-4-phenyL
  • quinazoL
  • 2-CHLORO-4-PHENYLQUINAZOLINE ISO 9001:2015 REACH
  • 2-CHLORO-4-PHENYLQUINAZOLINE
  • 2-Chloro-4-phenylq inazollne
CAS:
29874-83-7
MF:
C14H9ClN2
MW:
240.69
EINECS:
201-615-9
Product Categories:
  • quinazoline
Mol File:
29874-83-7.mol
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2-CHLORO-4-PHENYLQUINAZOLINE Chemical Properties

Melting point:
113.0 to 117.0 °C
Boiling point:
347.4±30.0 °C(Predicted)
Density 
1.285±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder to crystal
pka
0.24±0.30(Predicted)
color 
White to Orange to Green
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Safety Information

HS Code 
2933998090
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2-CHLORO-4-PHENYLQUINAZOLINE Usage And Synthesis

Uses

2-Chloro-4-phenylquinazoline acts as a reagent in the synthesis of MTH1 inhibitors that are potential cancer eradicators.

Uses

2-Chloro-4-phenylquinazoline acts as a reagent in the synthesis of MTH1 inhibitors that are potential cancer eradicators.

Uses

2-CHLORO-4-PHENYLQUINAZOLINE can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.

Synthesis


A 2 L flask was charged with 35.0 g (175.8 mmol) of 2,4-dichloroquinoline,22.5 g (184.6 mmol) of phenylboronic acid, 6.1 g (5.3 mmol) of tetrakis(triphenylphosphine)palladium(0) were added to 800 mL of tetrahydrofuran and 400 mL of water, and the mixture was heated to 60 ?? C for 12 hours under a nitrogen stream. . The resulting mixture was added to methanol (3000 mL), and the crystallized solid was filtered and dissolved in toluene, filtered through silica gel / celite, and the organic solvent was removed in an appropriate amount, and then recrystallization from methanol gave Intermediate I-A52-1 (36.8 g, 87% yield).

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