2-Hydrazino-4,6-dimethylpyrimidine
2-Hydrazino-4,6-dimethylpyrimidine Basic information
- Product Name:
- 2-Hydrazino-4,6-dimethylpyrimidine
- Synonyms:
-
- 2(1H)-Pyrimidinone, 4,6-dimethyl-, hydrazone (7CI,9CI)
- 4,6-Dimethyl-2-hydrazinopyrimidine
- 2-Hydrazino-4,6-dimethylpyrimidine
- 2-hydrazino-4,6-dimethylpyrimidine(SALTDATA: FREE)
- 2-Hydrazino-4
- 2(1H)-Pyrimidinone, 4,6-dimethyl-, hydrazone
- 2-hydrazineyl-4,6-dimethylpyrimidine
- 2-Hydrazino-4,6-dimethylpyrimidine Solution
- CAS:
- 23906-13-0
- MF:
- C6H10N4
- MW:
- 138.17
- Product Categories:
-
- PYRIMIDINE
- Mol File:
- 23906-13-0.mol
2-Hydrazino-4,6-dimethylpyrimidine Chemical Properties
- Melting point:
- 165 °C
- Boiling point:
- 256.0±23.0 °C(Predicted)
- Density
- 1.26±0.1 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Store in freezer, under -20°C
- solubility
- Chloroform (Slightly), Methanol (Slightly)
- form
- Solid
- pka
- 6.44±0.70(Predicted)
- color
- White to Off-White
2-Hydrazino-4,6-dimethylpyrimidine Usage And Synthesis
Synthesis
4472-44-0
23906-13-0
General procedure for the synthesis of 2-hydrazino-4,6-dimethylpyrimidines using 2-chloro-4,6-dimethylpyrimidines as starting material: hydrazine monohydrate (1.02 mL, 21.0 mmol) was slowly added to a solution of ethanol (5 mL) containing 2-chloro-4,6-dimethylpyrimidines (2 g, 14.0 mmol). The reaction mixture was stirred continuously for 2 hours at room temperature. Upon completion of the reaction, the precipitate precipitated was collected by vacuum filtration and washed with cold methanol. The resulting solid was dried under a stream of air to give 2-hydrazino-4,6-dimethylpyrimidine (1 g, 52% yield) as a white solid. The product was confirmed by mass spectrometry (ESI+) with a m/z of 139 (MH+).
References
[1] Patent: WO2012/154880, 2012, A1. Location in patent: Page/Page column 60
[2] Journal of the Chemical Society, 1952, p. 4691,4694
[3] Farmaco, Edizione Scientifica, 1956, vol. 11, p. 389,393
[4] Farmaco, Edizione Scientifica, 1983, vol. 38, # 4, p. 255 - 264
[5] Chemistry of Heterocyclic Compounds (New York, NY, United States), 1989, vol. 25, # 12, p. 1369 - 1373
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