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39136-60-2

39136-60-2 Structure

39136-60-2 Structure
IdentificationBack Directory
[Name]

5-Ethylthiazol-2-amine
[CAS]

39136-60-2
[Synonyms]

5-Ethylthiazol-2-amine
2-Thiazolamine, 5-ethyl-
2-Amino-5-(ethyl)thiazole
(5-Ethylthiazol-2-yl)amine
5-ethyl-1,3-thiazol-2-amine
[Molecular Formula]

C5H8N2S
[MDL Number]

MFCD00613421
[MOL File]

39136-60-2.mol
[Molecular Weight]

128.2
Chemical PropertiesBack Directory
[Melting point ]

59 °C
[Boiling point ]

241.9±9.0 °C(Predicted)
[density ]

1.195±0.06 g/cm3(Predicted)
[storage temp. ]

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

5.37±0.10(Predicted)
[Appearance]

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


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

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

5-Ethylthiazol-2-amine(39136-60-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Butyraldehyde

123-72-8

Urea

57-13-6

5-Ethylthiazol-2-amine

39136-60-2

5-Ethylthiazol-2-amine was synthesized as follows: n-butyraldehyde (10.8 g, 0.15 mol) was dissolved with urea (22.8 g, 0.3 mol) in chloroform (75 mL) at 0 °C, and sulfuryl chloride (13.5 mL, 0.166 mol) was added slowly and dropwise. The reaction mixture was gradually warmed to room temperature and stirred continuously for 1 hour. Subsequently, the solvent was removed by rotary evaporation. Ethanol (200 mL) was added to the residue and heated to reflux overnight before the solvent was removed by evaporation again. The resulting residue was suspended in water (200 mL) and the precipitate was collected by vacuum filtration to give 5-ethylthiazol-2-amine (9.5 g, 40% yield) as a light brown solid. Mass spectrometry analysis showed m/z 129.1 [M + H]+.

[References]

[1] Patent: US9617268, 2017, B2. Location in patent: Page/Page column 374
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