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2-Bromo-6-methoxybenzothiazole

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Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:2-bromo-6-methoxybenzo[d]thiazole
CAS:2941-58-4
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
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Products Intro: Product Name:2-bromo-6-methoxybenzo[d]thiazole
CAS:2941-58-4
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: Jinan Carbotang Biotech Co.,Ltd.
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Products Intro: Product Name:2-Bromo-6-methoxybenzothiazole
CAS:2941-58-4
Purity:98% Package:5KG;1KG
Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:2-Bromo-6-methoxybenzothiazole
CAS:2941-58-4
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-00953
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:2-bromo-6-methoxybenzothiazole
CAS:2941-58-4
Purity:0.99 Package:1kg

2-Bromo-6-methoxybenzothiazole manufacturers

2-Bromo-6-methoxybenzothiazole Basic information
Product Name:2-Bromo-6-methoxybenzothiazole
Synonyms:2-BROMO-6-METHOXYBENZOTHIAZOLE;Benzothiazole, 2-bromo-6-methoxy-;2-Bromo-6-methoxybenzothiazoL;2-bromo-6-methoxybenzo[d]thiazole
CAS:2941-58-4
MF:C8H6BrNOS
MW:244.11
EINECS:
Product Categories:Thiazole;Research
Mol File:2941-58-4.mol
2-Bromo-6-methoxybenzothiazole Structure
2-Bromo-6-methoxybenzothiazole Chemical Properties
Boiling point 335.4±34.0 °C(Predicted)
density 1.666±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka0.53±0.10(Predicted)
AppearanceLight yellow to orange Solid
Safety Information
HS Code 29342000
MSDS Information
2-Bromo-6-methoxybenzothiazole Usage And Synthesis
Uses2-Bromo-6-methoxybenzothiazole is used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.
SynthesisSynthesis_2941-58-4
2-Bromo-6-methoxybenzo[d]thiazole (B2) (Scheme 1). 6- Methoxybenzo[d]thiazol-2-amine (5.0 g; 27.7 mmol) was dissolved in 125 mL CHBCN. t- Butylnitrite (3.4 mL; 28 mmol) was added slowly. CuBr (5.0 g; 34.9 mmol) was added portion-wise through a funnel. The reaction was monitored by HPLC. After 3 hours, ethyl acetate (500 mL) was added, and the mixture was filtered through celite. The organic layer was washed with brine twice (200 mL each). The organic layer was dried over MgSO4. After filtration, the solvent was removed. The residual was dissolved in 50 mL CH2Cl2, and 2 g of silica gel was added. After drying, the silica gel loaded on a silica gel cake in hexane. The product was eluted with 5% ethyl acetate and 95% hexane. A yellowish band was collected (1.5 L). The solvent was removed to afford the product. Yield: 0.81 g 12%.
References[1] Chemistry - A European Journal, 2016, vol. 22, # 27, p. 9330 - 9337
[2] Patent: JP6095208, 2017, B2. Location in patent: Paragraph 0027; 0028; 0029
[3] Patent: US2009/275624, 2009, A1. Location in patent: Page/Page column 22
[4] Chemical Communications, 2016, vol. 52, # 75, p. 11199 - 11202
[5] Patent: KR101659952, 2016, B1. Location in patent: Paragraph 0219; 0221
2-Bromo-6-methoxybenzothiazole Preparation Products And Raw materials
Raw materials2-Amino-6-methoxybenzothiazole-->Cupric bromide-->Acetonitrile-->Isobutyl nitrite
Preparation Products2-Cyano-6-methoxybenzothiazole
Tag:2-Bromo-6-methoxybenzothiazole(2941-58-4) Related Product Information
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