Basic information Safety Supplier Related

5-Bromo-2-mercaptobenzothiazole

Basic information Safety Supplier Related

5-Bromo-2-mercaptobenzothiazole Basic information

Product Name:
5-Bromo-2-mercaptobenzothiazole
Synonyms:
  • 5-Bromo-2-mercaptobenzothiazole
  • 5-CHLORO-BENZOTHIAZOLE-2-THIOL
  • 5-CHLORO-1,3-BENZOTHIAZOLE-2-THIOL
  • TIMTEC-BB SBB005398
  • 5-BROMO-2-MERCAPTO BENZOTHLAZOLE
  • 5-Bromo-2-Thiobenzothiazole
  • 5-BROMO-2-MERCAPTO BENZIMIDAZOLE
  • 5-broMo-1,3-benzothiazole-2-thiol
CAS:
71216-20-1
MF:
C7H4BrNS2
MW:
246.15
EINECS:
226-235-0
Product Categories:
  • Heterocycles
  • Heterocyclic Compound
Mol File:
71216-20-1.mol
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5-Bromo-2-mercaptobenzothiazole Chemical Properties

Melting point:
198-200 °C(lit.)
storage temp. 
2-8°C
Appearance
Yellow to brown Solid
CAS DataBase Reference
71216-20-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
36/37/38-20/21/22
Safety Statements 
36/37/39-26-22
WGK Germany 
3
RTECS 
DL6490000

MSDS

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5-Bromo-2-mercaptobenzothiazole Usage And Synthesis

Chemical Properties

Yellow solid

Synthesis

768-11-6

71216-20-1

General procedure for the synthesis of 5-bromo-2-mercaptobenzothiazole from 5-bromobenzothiazole: 5-bromobenzothiazole (214.08 mg, 1.0 mmol), 1,3-propanedithiol (325 μL, 3.0 mmol), potassium carbonate (552 mg, 4.0 mmol), and DMSO (2 mL) were added into a reaction tube equipped with a magnetic stirrer. The reaction system was displaced three times with nitrogen to remove air, followed by stirring the reaction for 12 h in an oil bath at 120 °C. Upon completion of the reaction, the reaction mixture was transferred to a dispensing funnel and washed with an appropriate amount of water. The pH of the aqueous phase was adjusted to 1-3 with dilute hydrochloric acid, followed by extraction of the organic phase with dichloromethane. The organic phases were combined and dried with anhydrous magnesium sulfate. After filtration, the organic phase was concentrated under reduced pressure and the resulting crude product was purified by column chromatography to give a pink solid product (112.4 mg, 45.7% yield).

References

[1] Patent: CN108530374, 2018, A. Location in patent: Paragraph 0032; 0033

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