8-Fluoro-4-chromanone

8-Fluoro-4-chromanone Suppliers list
Company Name: Accela ChemBio Co.,Ltd.  Gold
Tel: 021-50795510 4000665055
Email: marketing@accelachem.com
Company Name: PharmaBlock Sciences (Nanjing),Inc.  
Tel: 025-86918202 4000255188
Email: sales@pharmablock.com
Company Name: Capot Chemical Co., Ltd  
Tel: +86 (0) 571 85 58 67 18
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Company Name: Shanghai Yuanding Chem. Sci. & Tech. Co., Ltd.  
Tel: 21-57721279 18121011378
Email: sales@shydchem.com.cn
Company Name: Shanghai Paulshine Chemical Co., Ltd.  
Tel: +86-021-37788663
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8-Fluoro-4-chromanone manufacturers

8-Fluoro-4-chromanone Basic information
Product Name:8-Fluoro-4-chromanone
Synonyms:5-fluoro-3,4-dihydro-2H-1-benzopyran-4-one;8-fluoro-2,3-dihydrochroMen-4-one;8-fluoro-3,4-dihydro-2H-1-benzopyran-4-one;8-Fluoro-4-chromanone;8-FLUORO-4-OXO-CHROMAN;8-Fluoro-2,3-dihydro-4H-chromen-4-one;8-fluorochroman-4-one;8-Fluoro-2,3-dihydro-4H-chromen-4-o
CAS:111141-00-5
MF:C9H7FO2
MW:166.15
EINECS:
Product Categories:Fused Ring Systems
Mol File:111141-00-5.mol
8-Fluoro-4-chromanone Structure
8-Fluoro-4-chromanone Chemical Properties
Melting point 84-87 °C
Boiling point 280.0±40.0 °C(Predicted)
density 1.297±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
AppearanceWhite to off-white Solid
InChIInChI=1S/C9H7FO2/c10-7-3-1-2-6-8(11)4-5-12-9(6)7/h1-3H,4-5H2
InChIKeyFKDMFDMYQZIZMI-UHFFFAOYSA-N
SMILESC1OC2=C(F)C=CC=C2C(=O)C1
Safety Information
HS Code 2932990090
MSDS Information
8-Fluoro-4-chromanone Usage And Synthesis
Synthesis
3-(2-FLUORO-PHENOXY)-PROPIONIC ACID

2967-72-8

8-Fluoro-4-chromanone

111141-00-5

General procedure for the synthesis of 8-fluorobenzodihydropyran-4-one from 3-(2-fluorophenoxy)propionic acid: oxalyl chloride (8.79 mL) and 1 drop of N,N-dimethylformamide (DMF) were added to a solution of 3-(2-fluorophenoxy)propionic acid (9.27 g) in dichloromethane (DCM, 50 mL) under ice-bath conditions. The reaction mixture was stirred at 0 °C for 2 h. Aluminum chloride (7.39 g, 55.42 mmol) was subsequently added. The reaction mixture was continued to be stirred at room temperature for 16 hours. After completion of the reaction, the mixture was poured into ice water and extracted three times with dichloromethane (DCM). The organic phases were combined and washed sequentially with 0.5 M sodium hydroxide (NaOH) solution and saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by column chromatography with the eluent of 20% ethyl acetate (EtOAc)/hexane (Hex) to afford the target product 8-fluorobenzodihydropyran-4-one (8.20 g, 98% yield).

References[1] Patent: WO2006/108103, 2006, A1. Location in patent: Page/Page column 95; 96
[2] Patent: US2008/119496, 2008, A1. Location in patent: Page/Page column 12; 30
[3] Journal of Medicinal Chemistry, 1988, vol. 31, # 1, p. 230 - 243
[4] Patent: EP2913330, 2015, A1. Location in patent: Paragraph 0653
[5] Patent: WO2006/66950, 2006, A2. Location in patent: Page/Page column 33-36
8-Fluoro-4-chromanone Preparation Products And Raw materials
Raw materials3-(2-FLUORO-PHENOXY)-PROPIONIC ACID-->Oxalyl chloride-->Dichloromethane-->Aluminum chloride
Tag:8-Fluoro-4-chromanone(111141-00-5) Related Product Information
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