ChemicalBook--->CAS DataBase List--->62484-29-1

62484-29-1

62484-29-1 Structure

62484-29-1 Structure
IdentificationBack Directory
[Name]

2,4,8-TRICHLOROQUINAZOLINE
[CAS]

62484-29-1
[Synonyms]

2,4,8-TRICHLOROQUINAZOLINE
Quinazoline, 2,4,8-trichloro-
[Molecular Formula]

C8H3Cl3N2
[MDL Number]

MFCD09954870
[MOL File]

62484-29-1.mol
[Molecular Weight]

233.48
Chemical PropertiesBack Directory
[Boiling point ]

309.1±24.0 °C(Predicted)
[density ]

1.60
[storage temp. ]

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

-1.68±0.30(Predicted)
[Appearance]

White to 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
[HS Code ]

2933599590
Spectrum DetailBack Directory
[Spectrum Detail]

2,4,8-TRICHLOROQUINAZOLINE(62484-29-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,4(1H,3H)-Quinazolinedione, 8-chloro-

62484-22-4

2,4,8-TRICHLOROQUINAZOLINE

62484-29-1

General procedure for the synthesis of 2,4,8-trichloroquinazoline from 8-chloroquinazoline-2,4(1H,3H)-dione: (1041) To 8-chloroquinazoline-2,4(1H,3H)-dione (3.8 g, 19.33 mmol) was added 60 mL of phosphorus oxychloride (POCl3). The reaction mixture was heated to reflux for 16 hours. Upon completion of the reaction, the excess phosphorous trichloride was evaporated under reduced pressure and the residue was purified by column chromatography to afford 2,4,8-trichloroquinazoline (3.11 g, 76% yield). Mass spectrum (ESI+): m/z = 233 [M + 1].

[References]

[1] Patent: US2016/168140, 2016, A1. Location in patent: Paragraph 1041
[2] Journal of Medicinal Chemistry, 2007, vol. 50, # 10, p. 2297 - 2300
[3] Patent: US5688803, 1997, A
[4] Patent: EP2226315, 2010, A1. Location in patent: Page/Page column 33
[5] Journal of Medicinal Chemistry, 2014, vol. 57, # 12, p. 5141 - 5156
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