ChemicalBook--->CAS DataBase List--->28969-60-0

28969-60-0

28969-60-0 Structure

28969-60-0 Structure
IdentificationBack Directory
[Name]

4-Amino-2,5,6-trichloropyrimidine
[CAS]

28969-60-0
[Synonyms]

2,5,6-TrichloropyriMidin-4-aMine
2,5,6-trichloro-4-pyrimidinamine
4-Amino-2,5,6-Trichloropyrimidine
4-Pyrimidinamine, 2,5,6-trichloro-
2,5,6-Trichloro-pyrimidin-4-ylamine
[Molecular Formula]

C4H2Cl3N3
[MDL Number]

MFCD09744035
[MOL File]

28969-60-0.mol
[Molecular Weight]

198.44
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[Appearance]

White to off-white 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-Amino-2,5,6-trichloropyrimidine(28969-60-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Amino-2,6-dichloropyrimidine

10132-07-7

4-Amino-2,5,6-trichloropyrimidine

28969-60-0

The general procedure for the synthesis of 4-amino-2,5,6-trichloropyrimidine from 4-amino-2,6-dichloropyrimidine was as follows: 1 g (6.1 mmol) of 4-amino-2,6-dichloropyrimidine was dissolved in 5 ml of N,N-dimethylformamide (DMF). To this solution 0.98 g (7.32 mmol) of N-chlorosuccinimide (NCS) was added. The reaction mixture was poured into 100 ml of ice water. The precipitate formed was collected by filtration, washed several times with distilled water and dried under vacuum to give 1.4 g (80% yield) of the target product as a white solid. The structure of the product was confirmed by 1H nuclear magnetic resonance (NMR) spectrum (300 MHz, DMSO-d6): δ= 8.24 (d, 2H).

[References]

[1] Patent: WO2011/121418, 2011, A1. Location in patent: Page/Page column 24-25
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