Basic information Safety Supplier Related

2-chloro-5-aminomethylthiazole

Basic information Safety Supplier Related

2-chloro-5-aminomethylthiazole Basic information

Product Name:
2-chloro-5-aminomethylthiazole
Synonyms:
  • 2-chloro-5-aminomethylthiazole
  • 5-Aminomethyl-2-chlorothiazole
  • (2-chloro-1,3-thiazol-5-yl)MethanaMine
  • 5-ThiazoleMethanaMine, 2-chloro-
  • 2-Chloro-5-Aomethylthiazole
  • 2-Chloro-5-thiazoleMethanaMine HCl
  • 2-Chloro-5-thiazolemethanamine
  • 1-(2-Chloro-1,3-thiazol-5-yl)methanamine
CAS:
120740-08-1
MF:
C4H5ClN2S
MW:
148.61
Product Categories:
  • Thiazole
  • Thiazoles
Mol File:
120740-08-1.mol
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2-chloro-5-aminomethylthiazole Chemical Properties

Melting point:
121 °C
Boiling point:
274.7±32.0 °C(Predicted)
Density 
1.427±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
solubility 
Chloroform (Slightly), Methanol (Slightly)
pka
7.68±0.29(Predicted)
form 
Oil
color 
Colourless to Yellow
Stability:
Hygroscopic
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2-chloro-5-aminomethylthiazole Usage And Synthesis

Uses

(2-Chlorothiazol-5-yl)methanamine is a metabolite of Thiamethoxam (T344180), a neonicotinoid insecticide.

Synthesis

120740-09-2

120740-08-1

General procedure for the synthesis of (2-chlorothiazol-5-yl)methanamine using 2-((2-chlorothiazol-5-yl)methyl)isodihydroindole-1,3-dione as starting material: 25.3 g of the above off-white solid and 150 mL of ethanol were added to a 250 mL three-necked flask in a unit equipped with a magnetic stirrer, a condenser tube and a drying tube. 9.1 g of hydrazine hydrate was slowly added dropwise to the reaction system. Subsequently, the reaction mixture was heated to reflux for 4-6 hours. Upon completion of the reaction, the solvent was evaporated under reduced pressure to afford 9.1 g of (2-chlorothiazol-5-yl)methylamine, the product was in the form of an orange oil.

References

[1] Patent: US2015/51402, 2015, A1. Location in patent: Page/Page column 0075

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