Identification | Back Directory | [Name]
2-ThiazolaMine, 4-(4-chloro-2-thienyl)- | [CAS]
570407-10-2 | [Synonyms]
Avatrombopag Impurity 8 4-(4-Chloro-2-thienyl)-2-thiazolamine 2-ThiazolaMine, 4-(4-chloro-2-thienyl)- 4-(4-Chlorothiophen-2-yl)thiazol-2-amine 2-Amino-4-(4-chlorothiophen-2-yl)thiazole 4-(4-chlorothiophen-2-yl)-1,3-thiazol-2-amine 2-ThiazolaMine, 4-(4-chloro-2-thienyl)- 2-ThiazolaMine 2-ThiazolaMine, 4-(4-chloro-2-thienyl)- 2-ThiazolaMine, 4-(4-chloro-2-thienyl)- | [EINECS(EC#)]
1312995-182-4 | [Molecular Formula]
C7H5ClN2S2 | [MDL Number]
MFCD24627156 | [MOL File]
570407-10-2.mol | [Molecular Weight]
216.711 |
Hazard Information | Back Directory | [Uses]
4-(4-Chloro-2-thienyl)-2-thiazolamine can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development processes and chemical production processes. | [Synthesis]
Bromine was added to an ether solution of 4-chloro-2-acetylthiophene under ice cooling, and the mixture was stirred at room temperature for 2 hours to obtain a brominated compound. Thiourea was added to an EtOH solution of the brominated compound at room temperature, and the mixture was stirred overnight at 80??C to obtain 2-amino-4-(4-chlorothiophen-2-yl)thiazole. |
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