Basic information Safety Supplier Related

2-Benzothiazolamine,7-chloro-(9CI)

Basic information Safety Supplier Related

2-Benzothiazolamine,7-chloro-(9CI) Basic information

Product Name:
2-Benzothiazolamine,7-chloro-(9CI)
Synonyms:
  • 2-Amino-7-chlorobenzothiazole
  • 7-Chlorobenzothiazol-2-amine
  • 7-Chlorobenzo[d]thiazol-2-aMine
  • 2-Benzothiazolamine,7-chloro-(9CI)
  • 7-Chloro-benzothiazol-2-ylamine
  • 7-Chloro-1,3-benzothiazol-2-amine
  • 7-Chlorobenzo[d]thiazole-2-amine, 97%
  • 2-Amino-7-chlorobenzothiazol
CAS:
20358-01-4
MF:
C7H5ClN2S
MW:
184.65
Product Categories:
  • BENZOTHIAZOLE
Mol File:
20358-01-4.mol
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2-Benzothiazolamine,7-chloro-(9CI) Chemical Properties

Melting point:
177-178 °C(Solv: ethanol (64-17-5))
Boiling point:
344.3±34.0 °C(Predicted)
Density 
1.532±0.06 g/cm3(Predicted)
storage temp. 
RT, protect from light
pka
2.68±0.30(Predicted)
Appearance
Light yellow to light brown Solid
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Safety Information

HS Code 
29342000
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2-Benzothiazolamine,7-chloro-(9CI) Usage And Synthesis

Synthesis

4947-89-1

20358-00-3

20358-01-4

General procedure for the synthesis of 2-amino-5-chlorobenzothiazole and 7-chlorobenzo[d]thiazol-2-amine from 3-chlorobenzothiourea: 3-chlorobenzothiourea (105 mg, 0.56 mmol) was dissolved in 10 mL of acetic acid. Benzyltrimethylammonium tribromide (329 mg, 0.84 mmol) was added and the reaction mixture was stirred at room temperature for 14 hours. After completion of the reaction, the acetic acid was removed by distillation under reduced pressure. The residue was redissolved in 15 mL of dichloromethane (DCM) and 10 mL of 0.5 N aqueous sodium hydroxide was added. The aqueous phase was extracted with dichloromethane (2 x 15 mL). The organic layers were combined, filtered through a phase separator and concentrated under reduced pressure to remove the solvent. The crude product was purified by fast column chromatography using pentane-ethyl acetate (12:5) as eluent to afford the target product 2-amino-5-chlorobenzothiazole (61 mg, 59% yield) as a white solid. The structure of the product was analyzed by 1H NMR (500 MHz, CD3OD) δ 7.05 (dd, J = 8.4, 2.0 Hz, 1H), 7.35 (d, J = 2.0 Hz, 1H), 7.53 (d, J = 8.4 Hz, 1H); 13C NMR (125 MHz, CD3OD) δ 117.41, 121.45, 121.60 129.37, 131.55, 153.24, 170.04; Mass Spectrometry (ESI): m/z 185 [M + H]+ confirmed.

References

[1] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 14, p. 4839 - 4843
[2] Yakugaku Zasshi, 1957, vol. 77, p. 649,651
[3] Chem.Abstr., 1957, p. 16435

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