2-chloro-5-aminomethylthiazole
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
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
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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2-chloro-5-aminomethylthiazole(120740-08-1)Related Product Information
- 2-Chlorothiazole
- 4-[(2-CHLORO-1,3-THIAZOL-5-YL)METHYL]MORPHOLINE
- 1-[(2-CHLORO-1,3-THIAZOL-5-YL)METHYL]-4-METHYLPIPERAZINE
- 1-[(2-CHLORO-1,3-THIAZOL-5-YL)METHYL]PIPERIDINE
- 2-CHLORO-5-(1H-PYRAZOL-1-YLMETHYL)-1,3-THIAZOLE
- 1-[(2-CHLORO-1,3-THIAZOL-5-YL)METHYL]-1H-INDOLE
- 2-[(2-CHLORO-1,3-THIAZOL-5-YL)METHYL]-1,2,3,4-TETRAHYDROISOQUINOLINE
- 1-[(2-CHLORO-1,3-THIAZOL-5-YL)METHYL]-1,2,3,4-TETRAHYDROQUINOLINE
- 1-[(2-CHLORO-1,3-THIAZOL-5-YL)METHYL]-4-(2-FLUOROPHENYL)PIPERAZINE
- N-[(2-CHLORO-1,3-THIAZOL-5-YL)METHYL]-3-METHOXY-1-PROPANAMINE
- 1-[(2-CHLORO-1,3-THIAZOL-5-YL)METHYL]-4-[3-(TRIFLUOROMETHYL)PHENYL]PIPERAZINE
- N-BENZYL(2-CHLORO-1,3-THIAZOL-5-YL)-N-METHYLMETHANAMINE
- 1-BENZYL-4-[(2-CHLORO-1,3-THIAZOL-5-YL)METHYL]PIPERAZINE
- 2-[(4-CHLOROBENZYLIDENE)AMINO]-3-([(2,4-DICHLORO-1,3-THIAZOL-5-YL)METHYL]AMINO)BUT-2-ENEDINITRILE
- 2-(BENZYLIDENEAMINO)-3-([(2,4-DICHLORO-1,3-THIAZOL-5-YL)METHYL]AMINO)BUT-2-ENEDINITRILE
- 1-[(2-CHLORO-1,3-THIAZOL-5-YL)METHYL]-4-PHENYLPIPERAZINE
- 2-[(2,6-DICHLOROBENZYLIDENE)AMINO]-3-([(2,4-DICHLORO-1,3-THIAZOL-5-YL)METHYL]AMINO)BUT-2-ENEDINITRILE
- 2-CHLORO-5-(1H-IMIDAZOL-1-YLMETHYL)-1,3-THIAZOLE