ChemicalBook--->CAS DataBase List--->625080-60-6

625080-60-6

625080-60-6 Structure

625080-60-6 Structure
IdentificationBack Directory
[Name]

4-CHLORO-6,7-DIFLUOROQUINAZOLINE
[CAS]

625080-60-6
[Synonyms]

Quinazoline, 4-chloro-6,7-difluoro-
[Molecular Formula]

C8H3ClF2N2
[MDL Number]

MFCD06657230
[MOL File]

625080-60-6.mol
[Molecular Weight]

200.57
Chemical PropertiesBack Directory
[Boiling point ]

290.9±35.0 °C(Predicted)
[density ]

1.538±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

-0.04±0.70(Predicted)
[Appearance]

White to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

4-CHLORO-6,7-DIFLUOROQUINAZOLINE(625080-60-6)1HNMR
4-CHLORO-6,7-DIFLUOROQUINAZOLINE(625080-60-6)1HNMR
4-CHLORO-6,7-DIFLUOROQUINAZOLINE(625080-60-6)19FNMR
Hazard InformationBack Directory
[Synthesis]

6,7-Difluoroquinazolin-4-ol

205259-37-6

4-CHLORO-6,7-DIFLUOROQUINAZOLINE

625080-60-6

Example 4A Step 2: 6,7-difluoro-4-hydroxyquinazoline (910 mg, 5 mmol) was added to trichlorophos (15 mL) followed by triethylamine (700 μL, 5 mmol). The reaction mixture was heated to reflux at 100 °C for 4 h. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. The resulting solid was ground with ethyl acetate (2 × 100 mL), and the combined organic phases were rapidly filtered through a silica gel column to afford 4-chloro-6,7-difluoroquinazoline (870 mg, 4.35 mmol, 87% yield). m/z 201 ([M + H]+) by LC-MS (ESI).

[References]

[1] Patent: WO2009/117080, 2009, A1. Location in patent: Page/Page column 165
[2] Patent: US2006/281772, 2006, A1. Location in patent: Page/Page column 131
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