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2-BROMO-4-CHLOROBENZOTHIAZOLE

2-BROMO-4-CHLOROBENZOTHIAZOLE Suppliers list
Company Name: Shaanxi Dideu Medichem Co. Ltd
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Email: 1057@dideu.com
Products Intro: Product Name: 2-BROMO-4-CHLOROBENZOTHIAZOLE
CAS:3622-40-0
Purity:99% Package:1KG;1USD
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
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Products Intro: Product Name:2-bromo-4-chlorobenzo[d]thiazole
CAS:3622-40-0
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:2-Bromo-4-chlorobenzo[d]thiazole
CAS:3622-40-0
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-01970
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Products Intro: Product Name:2-BROMO-4-CHLOROBENZOTHIAZOLE
CAS:3622-40-0
Purity:99.0% Package:1KG;1USD
Company Name: Dideu Industries Group Limited
Tel: +86-29-89586680 +86-15129568250
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Products Intro: Product Name:2-Bromo-4-chlorobenzo[d]thiazole
CAS:3622-40-0
Purity:99.9% Package:25kgs/Drum;200kgs/Drum Remarks:FDA GMP CEP Approved Manufacturer

2-BROMO-4-CHLOROBENZOTHIAZOLE manufacturers

2-BROMO-4-CHLOROBENZOTHIAZOLE Basic information
Product Name:2-BROMO-4-CHLOROBENZOTHIAZOLE
Synonyms:2-BROMO-4-CHLOROBENZOTHIAZOLE;Benzothiazole, 2-bromo-4-chloro-;2-broMo-4-chlorobenzo[d]thiazole;2-broMo-4-chloro-1,3-benzothiazole;2-Bromo-4-chlorobenzo[d]thiazole USP/EP/BP
CAS:3622-40-0
MF:C7H3BrClNS
MW:248.53
EINECS:222-822-0
Product Categories:
Mol File:3622-40-0.mol
2-BROMO-4-CHLOROBENZOTHIAZOLE Structure
2-BROMO-4-CHLOROBENZOTHIAZOLE Chemical Properties
Melting point 107-108 °C
Boiling point 330.5±34.0 °C(Predicted)
density 1.849±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka-2.02±0.10(Predicted)
AppearanceLight yellow to yellow Solid
Safety Information
HS Code 29342000
MSDS Information
2-BROMO-4-CHLOROBENZOTHIAZOLE Usage And Synthesis
Synthesis
2-AMINO-4-CHLOROBENZOTHIAZOLE

19952-47-7

2-BROMO-4-CHLOROBENZOTHIAZOLE

3622-40-0

GENERAL METHOD: To a stirred suspension of CuBr (1.57 g, 10.9 mmol) in acetonitrile (25 mL) was added tert-butyl nitrite (tBuONO, 1.63 mL, 13.7 mmol) and the mixture was stirred for 10 min at 60 °C. Subsequently, 2-amino-4-chlorobenzothiazole (1.50 g, 9.13 mmol) was added to the above mixture and the reaction continued to be stirred at 60 °C for 1 hour. After completion of the reaction, the mixture was cooled to room temperature and poured into 1N hydrochloric acid. The resulting precipitate was collected, dissolved in ethyl acetate (EtOAc), washed sequentially with 1N hydrochloric acid and saturated brine, dried over anhydrous sodium sulfate and subsequently concentrated under reduced pressure. The crude product was purified by silica gel column chromatography using n-hexane-ethyl acetate (7:1, v/v) as eluent, resulting in 2-bromo-4-chlorobenzothiazole (703 mg, 34% yield) as a brown oil.

References[1] Chemistry - A European Journal, 2018, vol. 24, # 55, p. 14622 - 14626
[2] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 3, p. 1201 - 1212
[3] Patent: WO2018/13774, 2018, A1. Location in patent: Page/Page column 685
[4] Organic Letters, 2015, vol. 17, # 15, p. 3722 - 3725
2-BROMO-4-CHLOROBENZOTHIAZOLE Preparation Products And Raw materials
Raw materials2-AMINO-4-CHLOROBENZOTHIAZOLE-->tert-Butyl nitrite-->Cuprous bromide-->Acetonitrile
Tag:2-BROMO-4-CHLOROBENZOTHIAZOLE(3622-40-0) Related Product Information
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