5-Bromo-2-mercaptobenzothiazole
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
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)
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
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
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
5-Bromo-2-mercaptobenzothiazoleSupplier
- Tel
- +86 351 7031519
- sales@RHFChem.com
- Tel
- 021-021-58432009 400-005-6266
- sales8178@energy-chemical.com
- Tel
- +86 (0) 571 85 58 67 18
- Tel
- 13817811078
- sales@jingyan-chemical.com
- Tel
- 001-857-928-2050 or 1-888-588-9418
- sales@chemreagents.com
5-Bromo-2-mercaptobenzothiazole(71216-20-1)Related Product Information
- 2,2'-Dithiobis(benzothiazole)
- 2-Mercaptothiazole
- 3-Bromoanisole
- Calcium thioglycolate
- Mercaptoacetic acid
- Sodium thioglycolate
- 3-Mercaptopropionic acid
- 2-Mercaptobenzothiazole
- 2-Ethylhexyl mercaptoacetate
- Benzothiazole
- Sodium mercaptobenzothiazole
- Bromine
- 2-Mercaptoethanol
- 5-Bromobenzothiazole
- Thiazole
- 5-CHLOROBENZOXAZOLE
- 6-Bromo-2-mercaptobenzothiazole
- 4-Bromo-2-mercaptobenzothiazole