6-Fluoro-2(3H)-benzothiazolone

6-Fluoro-2(3H)-benzothiazolone Suppliers list
Company Name: Xinyi Guangbang Medical Technology Co., Ltd.  Gold
Tel: 13361936468
Email: 410756539@qq.com
Company Name: JinYan Chemicals(ShangHai) Co.,Ltd.  
Tel: 13817811078
Email: sales@jingyan-chemical.com
Company Name: Shanghai Longsheng chemical Co.,Ltd.  
Tel: 58099637 13585536065
Email: sales@shlschem.com
Company Name: China DongFan Chemical Co.,LTD  
Tel: 86-0571-85151182
Email:
Company Name: China Langchem Inc.  
Tel: 0086-21-58956006
Email:

6-Fluoro-2(3H)-benzothiazolone manufacturers

6-Fluoro-2(3H)-benzothiazolone Basic information
Product Name:6-Fluoro-2(3H)-benzothiazolone
Synonyms:6-Fluoro-3H-benzothiazol-2-one;6-fluorobenzo[d]thiazol-2(3H)-one;6-Fluoro-2-hydroxybenzothiazole;2(3H)-Benzothiazolone,6-fluoro-(9CI);6-fluoro-3H-1,3-benzothiazol-2-one;6-Fluorobenzothiazolone;2(3H)-Benzothiazolone, 6-fluoro-;6-Fluoro-1,3-benzothiazol-2-ol
CAS:63754-96-1
MF:C7H4FNOS
MW:169.18
EINECS:
Product Categories:BENZOTHIAZOLE
Mol File:63754-96-1.mol
6-Fluoro-2(3H)-benzothiazolone Structure
6-Fluoro-2(3H)-benzothiazolone Chemical Properties
Melting point 188.4 °C
density 1.474±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka9.26±0.20(Predicted)
AppearanceWhite to yellow Solid
Safety Information
HS Code 2934999090
MSDS Information
6-Fluoro-2(3H)-benzothiazolone Usage And Synthesis
Chemical PropertiesWhite solid
Synthesis
Carbamic acid, N-(4-fluoro-2-iodophenyl)-, ethyl ester

1373399-24-6

6-FLUORO-2(3H)-BENZOTHIAZOLONE

63754-96-1

General procedure for the synthesis of 6-fluorobenzothiazol-2-one using the compound (CAS:1373399-24-6) as starting material: ethyl 2-iodophenylcarbamate (1 mmol), cuprous iodide (CuI, 19 mg, 0.1 mmol), and sodium sulfide hydrate nine (Na2S-9H2O, 3 mmol) were added sequentially to a Schlenk tube. The reaction system was evacuated and displaced with argon (repeated 3 times), and then N,N-dimethylformamide (DMF, 2 mL) was added. The reaction mixture was stirred at 80 °C for 10 to 16 hours. Upon completion of the reaction, acetic acid (AcOH, 3 mL) was added to the cooled reaction mixture and the mixture was continued to be stirred at 130°C for 36 hours. At the end of the reaction, saturated sodium bicarbonate solution (10 mL) was added for neutralization, followed by extraction of the reaction mixture with ethyl acetate. The organic layers were combined, washed sequentially with water, saturated saline and dried with anhydrous sodium sulfate (Na2SO4). After the solvent was removed by distillation under reduced pressure, the resulting crude product was purified by silica gel column chromatography to finally obtain the target product 6-fluorobenzothiazol-2-one.

References[1] Tetrahedron Letters, 2012, vol. 53, # 20, p. 2511 - 2513
6-Fluoro-2(3H)-benzothiazolone Preparation Products And Raw materials
Raw materialsCarbamic acid, N-(4-fluoro-2-iodophenyl)-, ethyl ester-->Acetic acid-->N,N-Dimethylformamide-->Copper(l) iodide-->Sodium sulfide nonahydrate
Tag:6-Fluoro-2(3H)-benzothiazolone(63754-96-1) Related Product Information
2-Hydroxy-4-methyl-benzothiozole 2-Amino-4,6-dichlorobenzothiazole 5-CHLOROBENZOTHIAZOLE 5-Bromo-2-mercaptobenzothiazole 2-Benzothiazolol 6-BROMO-2-BENZOTHIAZOLINONE 6-METHYL-3H-BENZOTHIAZOL-2-ONE 4-Choro-2(3H)-benzothiazolone 6-CHLORO-3H-BENZOTHIAZOL-2-ONE 5--fluoro-2(3H)-benzothiazolone 5-BROMO-2(3H)-BENZOTHIAZOLONE 2(3H)-Benzothiazolone,7-chloro-(9CI) 6-METHOXY-2(3H)-BENZOTHIAZOLONE 4-Fluoro-2(3H)-benzothiazolone 6-FLUORO-2(3H)-BENZOTHIAZOLONE 2-Amino-5-fluorobenzenethiol 2(3H)-Benzothiazolone,4,5,6,7-tetrafluoro-(9CI) 4,6-DIFLUORO-2(3H)-BENZOTHIAZOLONE