Identification | Back Directory | [Name]
2-AMINO-5-(2-CHLOROPHENYL)-1,3,4-THIADIAZOLE | [CAS]
828-81-9 | [Synonyms]
VITAS-BB TBB000090 5-(2-Chlorophenyl) IFLAB-BB F1386-0067 5-(2-CHLOROPHENYL)-1,3,4-THIADIAZOL-2-AMINE 2-AMINO-5-(2-CHLOROPHENYL)-1,3,4-THIADIAZOLE 1,3,4-Thiadiazol-2-aMine, 5-(2-chlorophenyl)- 5-(2-CHLORO-PHENYL)-[1,3,4]THIADIAZOL-2-YLAMINE | [Molecular Formula]
C8H6ClN3S | [MDL Number]
MFCD00548482 | [MOL File]
828-81-9.mol | [Molecular Weight]
211.67 |
Chemical Properties | Back Directory | [Melting point ]
192-195 °C | [Boiling point ]
393.8±44.0 °C(Predicted) | [density ]
1.461±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2–8 °C | [form ]
solid | [pka]
2.28±0.10(Predicted) | [Appearance]
Light yellow to brown Solid |
Hazard Information | Back Directory | [Synthesis]
5.1.1 Synthesis of 5-(2-chlorophenyl)-1,3,4-thiadiazol-2-amine (68): 2-chlorobenzoic acid (5.18 g, 25 mmol) and aminothiourea (2.28 g, 25 mmol) were dissolved in POCl3 (7 ml) and stirred vigorously for 0.5 hr at 75 °C. After completion of the reaction, H2O (30 ml) was added and the mixture was heated to reflux for 4 hours. Subsequently, the reaction mixture was adjusted with 50% NaOH solution to pH 8. The precipitate was collected by filtration and the filter cake was purified by recrystallization from ethanol to give the yellow crystalline product 68 in a yield of 3.90 g, 88% yield, melting point 190-192 °C (EtOH). The product was analyzed by ESI-MS, m/z: 212.1 [M + H]+; 1H NMR (CDCl3) δ 7.45-7.50 (m, 4H), 7.60-7.62 (m, 1H), 7.99-8.01 (m, 1H). Compounds 60-81 were synthesized in the same way. | [References]
[1] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1999, vol. 38, # 8, p. 998 - 1001 [2] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 21, p. 5766 - 5775 [3] Medicinal Chemistry Research, 2018, vol. 27, # 7, p. 1800 - 1821 [4] Medicinal Chemistry Research, 2012, vol. 21, # 6, p. 816 - 824 [5] Journal of Chemical Research, 2014, vol. 38, # 6, p. 347 - 350 |
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