Basic information Safety Supplier Related

4-(4-CHLORO-PHENYL)-5-METHYL-THIAZOL-2-YLAMINE

Basic information Safety Supplier Related

4-(4-CHLORO-PHENYL)-5-METHYL-THIAZOL-2-YLAMINE Basic information

Product Name:
4-(4-CHLORO-PHENYL)-5-METHYL-THIAZOL-2-YLAMINE
Synonyms:
  • 4-(4-chlorophenyl)-5-methyl-2-thiazolamine
  • 4-(4-CHLOROPHENYL)-5-METHYL-1,3-THIAZOL-2-AMINE
  • 4-(4-CHLORO-PHENYL)-5-METHYL-THIAZOL-2-YLAMINE
  • 4-(4-CHLOROPHENY)-5-METHYLTHIAZOL-2-YLAMINE
  • 4-(4-chlorophenyl)-5-methyl-1,3-thiazol-2-amine(SALTDATA: FREE)
  • 4-(4-Chlorophenyl)-5-Methylthiazol-2-aMine
  • CHEMBRDG-BB 3007469
  • 4-(4-chlorophenyl)-5-methyl-2-thiazol-3-idimine
CAS:
82632-77-7
MF:
C10H9ClN2S
MW:
224.71
Mol File:
82632-77-7.mol
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4-(4-CHLORO-PHENYL)-5-METHYL-THIAZOL-2-YLAMINE Chemical Properties

Melting point:
144-145℃ (hexane ethyl acetate )
Boiling point:
376.6±27.0 °C(Predicted)
Density 
1.338±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
soluble in Methanol
form 
powder to crystal
pka
4.43±0.10(Predicted)
color 
White to Yellow
CAS DataBase Reference
82632-77-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22-37/38-41
Safety Statements 
26-39
HS Code 
2934.10.2000
HazardClass 
IRRITANT
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4-(4-CHLORO-PHENYL)-5-METHYL-THIAZOL-2-YLAMINE Usage And Synthesis

Synthesis

6285-05-8

17356-08-0

82632-77-7

GENERAL METHOD: Thiourea (0.04 mol) and iodine (0.02 mol) were ground homogeneously in a mortar and subsequently mixed with 4-chloropropiophenone (0.02 mol). The reaction mixture was heated in a water bath at 70°C with intermittent stirring for 8 hours. Upon completion of the reaction, the solid product was ground to a fine powder and washed with ether to remove unreacted 4-chloropropiophenone. Next, it was washed with 5% aqueous sodium thiosulfate to remove residual iodine and finally with distilled water. The crude product was dissolved in hot water and hot filtered to remove insoluble impurities. Ammonia was slowly added to the filtrate until 2-amino-4-(4'-chlorophenyl)-5-methyl-1,3-thiazole precipitated completely. The precipitate was collected and recrystallized with ethanol to give purified crystals of the target compound [9].

References

[1] Asian Journal of Chemistry, 2017, vol. 29, # 12, p. 2794 - 2798
[2] Journal of the Indian Chemical Society, 1960, vol. 37, p. 427 - 428
[3] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 3, p. 313 - 317

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