Basic information Safety Supplier Related

6-Bromo-2-chlorobenzothiazole

Basic information Safety Supplier Related

6-Bromo-2-chlorobenzothiazole Basic information

Product Name:
6-Bromo-2-chlorobenzothiazole
Synonyms:
  • 6-Bromo-2-chlorobenzothiazole,97%
  • 6-Bromo-2-chlorobenzothiazole 97%
  • JR-8569, 6-Bromo-2-chlorobenzo[d]thiazole, 97%
  • 6-BROMO-2-CHLOROBENZO[D]THIAZOLE
  • 6-BROMO-2-CHLOROBENZOTHIAZOLE
  • 6-BROMO-2-CHLORO-1,3-BENZOTHIAZOLE
  • Benzothiazole, 6-bromo-2-chloro-
  • IFLAB-BB F1910-0018
CAS:
80945-86-4
MF:
C7H3BrClNS
MW:
248.53
EINECS:
627-810-2
Product Categories:
  • Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Thiazoles
  • ThiazolesHeterocyclic Building Blocks
Mol File:
80945-86-4.mol
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6-Bromo-2-chlorobenzothiazole Chemical Properties

Melting point:
99-103 °C
Boiling point:
157°C/18mmHg(lit.)
Density 
1.849±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
soluble in Toluene
form 
powder to crystal
pka
-0.87±0.10(Predicted)
color 
White to Orange to Green
CAS DataBase Reference
80945-86-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36/37/38
Safety Statements 
26-36
RIDADR 
UN 2811
WGK Germany 
3
HazardClass 
IRRITANT
PackingGroup 
HS Code 
29342000
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6-Bromo-2-chlorobenzothiazole Usage And Synthesis

Chemical Properties

White solid

Uses

Starting material in a synthesis of benzothiazole dimers with high binding affinity to β-amyloid fibrils.

Synthesis

62266-82-4

80945-86-4

General procedure for the synthesis of 6-bromo-2-chlorobenzothiazole from 6-bromo-2-benzothiazolone: 6-bromo-2-benzothiazolone (500 mg, 2.2 mmol) was dissolved in phosphorus trichloride (5 mL) and the reaction was carried out at reflux for 18 hours. After completion of the reaction, the reaction mixture was slowly poured into ice water. The pH of the mixture was adjusted to 9 with ammonia to neutralize the reaction. The resulting solid product was collected by filtration, washed with water and dried under vacuum to afford 6-bromo-2-chlorobenzothiazole (450 mg, 83% yield).

References

[1] Patent: WO2007/146066, 2007, A2. Location in patent: Page/Page column 88-89
[2] Patent: US2015/368278, 2015, A1. Location in patent: Paragraph 1050

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