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23906-13-0

23906-13-0 Structure

23906-13-0 Structure
IdentificationBack Directory
[Name]

2-Hydrazino-4,6-dimethylpyrimidine
[CAS]

23906-13-0
[Synonyms]

2-Hydrazino-4
4,6-Dimethyl-2-hydrazinopyrimidine
2-Hydrazino-4,6-dimethylpyrimidine
4,6-dimethyl-2-hydrazinylpyrimidine
2-hydrazineyl-4,6-dimethylpyrimidine
Pyrimidine, 2-hydrazinyl-4,6-dimethyl-
2-Hydrazino-4,6-dimethylpyrimidine Solution
2(1H)-Pyrimidinone, 4,6-dimethyl-, hydrazone
2-hydrazino-4,6-dimethylpyrimidine(SALTDATA: FREE)
2-Hydrazino-4,6-dimethylpyrimidine ISO 9001:2015 REACH
2(1H)-Pyrimidinone, 4,6-dimethyl-, hydrazone (7CI,9CI)
[Molecular Formula]

C6H10N4
[MDL Number]

MFCD00094479
[MOL File]

23906-13-0.mol
[Molecular Weight]

138.17
Chemical PropertiesBack Directory
[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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P280-P305+P351+P338-P310
[HS Code ]

2933599590
Spectrum DetailBack Directory
[Spectrum Detail]

2-Hydrazino-4,6-dimethylpyrimidine(23906-13-0)MS
2-Hydrazino-4,6-dimethylpyrimidine(23906-13-0)1HNMR
2-Hydrazino-4,6-dimethylpyrimidine(23906-13-0)IR1
2-Hydrazino-4,6-dimethylpyrimidine(23906-13-0)IR2
Hazard InformationBack Directory
[Synthesis]

2-Chloro-4,6-dimethylpyrimidine

4472-44-0

2-Hydrazino-4,6-dimethylpyrimidine

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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