Basic information Safety Supplier Related

2-Chlorobenzothiazo-6-amine

Basic information Safety Supplier Related

2-Chlorobenzothiazo-6-amine Basic information

Product Name:
2-Chlorobenzothiazo-6-amine
Synonyms:
  • 6-Amino-2-chlorobenzothiazole 97%
  • 2-CHLORO-BENZOTHIAZOL-6-YLAMINE
  • 6-Benzothiazolamine,2-chloro-(9CI)
  • 6-Benzothiazolamine, 2-chloro-
  • 2-CHLOROBENZOTHIAZO-6-AMINE
  • 2-Chloro-6-aminobenzothiazole
  • 6-Amino-2-chlorobenzothiazole
  • 2-CHLOROBENZOTHIAZO-6YL-AMINE
CAS:
2406-90-8
MF:
C7H5ClN2S
MW:
184.65
Product Categories:
  • BENZOTHIAZOLE
Mol File:
2406-90-8.mol
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2-Chlorobenzothiazo-6-amine Chemical Properties

Melting point:
155-157 °C
Boiling point:
337.3±15.0 °C(Predicted)
Density 
1.532
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
2.09±0.10(Predicted)
Appearance
Light brown to yellow Solid
InChI
InChI=1S/C7H5ClN2S/c8-7-10-5-2-1-4(9)3-6(5)11-7/h1-3H,9H2
InChIKey
YPTWPDOGEAHMOR-UHFFFAOYSA-N
SMILES
S1C2=CC(N)=CC=C2N=C1Cl
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Safety Information

HS Code 
29342000
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2-Chlorobenzothiazo-6-amine Usage And Synthesis

Synthesis

2407-11-6

2406-90-8

General procedure for the synthesis of 2-chloro-6-aminobenzothiazole from 2-chloro-6-nitrobenzothiazole: (B) Synthesis of 2-chloro-6-aminobenzothiazole (3) Compound 2 (1.96 g, 9.14 mmol) was dissolved in a solvent mixture of ethanol (150 mL) and purified water (100 mL), and anhydrous tin (II) chloride (20.7 g) was subsequently added to the solution (20.7 g, 91.7 mmol) was added to the solution. Next, a 4.8 mol/L hydrochloric acid solution (20 mL, 96 mmol) was added dropwise to the reaction mixture and the reaction was refluxed at 120 °C. The progress of the reaction was monitored by thin-layer chromatography (unfolding agent: dichloromethane), and after confirming the complete disappearance of the feedstock, the reaction mixture was alkalized with aqueous sodium hydroxide solution. The insoluble precipitate was removed by filtration and the filtrate was subsequently concentrated under reduced pressure. The residue was extracted three times with ethyl acetate, and the combined organic layers were washed with saturated brine, dried over anhydrous sodium sulfate, and finally concentrated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (eluent: ethyl acetate/hexane = 1/1) to afford compound 3 in white solid form (1.02 g, 61% yield).1H-NMR (300 MHz, CDCl3) δ 3.85 (br, 2H), 6.81 (dd, 1H, J = 2.4, 8.7 Hz), 6.99 (d, 1H, J = 2.4 Hz), 7.70 (d, 1H, J = 8.7 Hz). ms (ESI+) m/z 185.0 [M + H]+.

References

[1] Patent: WO2004/37251, 2004, A1. Location in patent: Page/Page column 99; 100
[2] Journal of the American Chemical Society, 2010, vol. 132, # 39, p. 13586 - 13587
[3] Patent: US2007/155806, 2007, A1. Location in patent: Page/Page column 5
[4] Chemistry - An Asian Journal, 2011, vol. 6, # 7, p. 1800 - 1810
[5] Chemical Communications, 2013, vol. 49, # 77, p. 8644 - 8646

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