Basic information Safety Supplier Related

2,4-Dichlorobenzothiazole

Basic information Safety Supplier Related

2,4-Dichlorobenzothiazole Basic information

Product Name:
2,4-Dichlorobenzothiazole
Synonyms:
  • 2,4-Dichlorbenzothiazol
  • Benzothiazole, 2,4-dichloro-
  • 2,4-Dichlorobenzo[d]thiazole
  • 2,4-DICHLOROBENZOTHIAZOLE
  • 2,4-DICHLORO-1,3-BENZOTHIAZOLE
  • IFLAB-BB F1910-0008
  • Benzothiazole, 2,4-dichloro- (7CI,8CI,9CI)
  • sulfuric acid [[3-hydroxy-1-oxo-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-mercapto-2-oxanyl]pent-4-enyl]amino] ester
CAS:
3622-30-8
MF:
C7H3Cl2NS
MW:
204.08
EINECS:
222-821-5
Product Categories:
  • BENZOTHIAZOLE
Mol File:
3622-30-8.mol
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2,4-Dichlorobenzothiazole Chemical Properties

Melting point:
96-97 °C
Boiling point:
286.8±13.0 °C(Predicted)
Density 
1.567±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-2.02±0.10(Predicted)
Appearance
Light yellow to orange Solid
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Safety Information

HS Code 
29342000
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2,4-Dichlorobenzothiazole Usage And Synthesis

Chemical Properties

Pale yellow solid

Synthesis

19952-47-7

3622-30-8

Step B: 4-Chlorobenzo[d]thiazol-2-amine (4.78 g, 25.8 mmol) and copper(II) chloride (4.16 g, 31 mmol) were dissolved in acetonitrile (25 mL), followed by tert-butyl nitrite (4.61 mL, 38.8 mmol) at room temperature. The reaction mixture was heated to 60 °C and maintained for 30 min. Upon completion of the reaction, the solvent was removed by rotary evaporation. The residue was suspended in water and the solid product was collected by filtration and dried to give 2,4-dichlorobenzo[d]thiazole (5.3 g, 81% yield). Mass spectrometry analysis showed a m/z of 205.9 [M + H]+.

References

[1] Chemistry - A European Journal, 2018, vol. 24, # 55, p. 14622 - 14626
[2] Patent: WO2013/101974, 2013, A1. Location in patent: Paragraph 00586; 00588
[3] Patent: US9617268, 2017, B2. Location in patent: Page/Page column 321; 322
[4] Gazzetta Chimica Italiana, 1964, vol. 94, p. 372 - 381
[5] Chemistry and Biodiversity, 2011, vol. 8, # 2, p. 253 - 265

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